77957687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: 5 prime UTR variant
orthologous variants: 117544602-A-G

77957724-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 117544634-C-G

77957976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117544880-C-T

http://identifiers.org/hco/17/GRCh38#77958256-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#117545192-A-C

77958320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, undefined
orthologous variants: 117545256-G-A

77958339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, undefined
orthologous variants: 117545273-G-A

http://identifiers.org/hco/17/GRCh38#77958472-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#117545405-A-C

77958472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, undefined
orthologous variants: 117545405-A-G

77958538-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, undefined
orthologous variants: 117545474-G-C

77958695-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, undefined
orthologous variants: 117545631-T-G

77958784-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 117545720-C-G

77958785-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 117545721-C-G

77958891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 117545822-C-T

77959160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 117546055-G-A

77959161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 117546056-C-T

77959260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 117546149-G-A

77959260-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 117546149-G-T

http://identifiers.org/hco/17/GRCh38#77959404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#117546252-C-A

77959404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117546252-C-T

77959688-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117546500-G-C

77959688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117546500-G-T

77959772-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117546570-C-G

77959772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117546570-C-T

77959825-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117546640-C-G

77959859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117546674-C-T

77960107-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117546935-T-G

77960373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117547212-T-C

77960690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117547493-C-T

77960971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117547744-C-T

77961120-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117547867-C-G

77961596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117548013-T-C

http://identifiers.org/hco/17/GRCh38#77962026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#117548380-C-A

77962628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117549141-G-T

77962695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117549210-T-C

77963160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117549617-T-C

77963177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117549634-A-G

77963445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117549803-C-T

77963515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117549871-G-A

77963592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117549952-A-G

77963835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117550145-G-T

77963839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117550149-A-G

77965124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117551615-G-A

77965232-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117551733-C-G

77965459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117551932-A-G

77965494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117551957-A-G

77965806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117552185-G-A

77965806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117552185-G-T

77966016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117552336-G-A

77966161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117552468-G-A

77966469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117552792-G-A

http://identifiers.org/hco/17/GRCh38#77966740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#117553041-C-A

77967146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117553594-G-T

77967825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117554586-C-T

http://identifiers.org/hco/17/GRCh38#77967839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#117554600-C-A

77967839-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117554600-C-G

77967985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117554707-A-G

77968245-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117555005-G-C

77968275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117555051-G-A

77968275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117555051-G-T

77968284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117555060-G-A

77969734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117555931-G-T

77970047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117556244-A-G

77970047-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117556244-A-T

77974661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117557532-A-G

77974757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117557632-A-G

77974875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117557793-G-A

http://identifiers.org/hco/17/GRCh38#77975200-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#117558305-A-C

77975200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117558305-A-G

77975535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117559096-G-T

77975620-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117559172-T-A

77976301-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117560550-A-T

77977056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117560980-A-G

77977081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117560999-T-C

77978089-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117563730-G-T

77978178-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117563800-T-A

77978178-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117563800-T-G

77978467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117564048-G-A

77978934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117564455-T-C

77979689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117565531-T-C

http://identifiers.org/hco/17/GRCh38#77979714-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#117565685-A-C

77979714-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117565685-A-T

77979939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117566038-A-G

77985660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117568944-G-A

77986628-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117570673-A-T

77986927-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117570935-C-G

77988614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117572594-T-C

77988720-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117572678-A-T

77988922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117573308-C-T

77989368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117573710-T-C

77989371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117573713-A-G

77989427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117573768-A-G

77989452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117573794-T-C

77993490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117574111-A-G

http://identifiers.org/hco/17/GRCh38#77993968-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#117575083-A-C

77994069-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, undefined
orthologous variants: 117575210-T-A

77994069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, undefined
orthologous variants: 117575210-T-C

77994134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117575266-A-G

77994336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117575423-G-A

77994398-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117575489-C-G

77994398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117575489-C-T

77994481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117575571-C-T

77995590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117576570-T-C

77999020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117577833-G-A

77999297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117578053-T-C

77999412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117578169-C-T

77999573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117578316-A-G

77999601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117578333-C-T

http://identifiers.org/hco/17/GRCh38#77999816-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#117578531-A-C

77999888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, undefined
orthologous variants: 117578604-G-A

77999888-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, undefined
orthologous variants: 117578604-G-C

http://identifiers.org/hco/17/GRCh38#78000477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#117579084-C-A

http://identifiers.org/hco/17/GRCh38#78000786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#117579371-C-A

78002129-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117583562-T-A

78002208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117583632-A-G

78002318-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117583758-A-T

http://identifiers.org/hco/17/GRCh38#78002753-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#117584187-C-A

78002774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117584207-A-G

78002805-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117584224-T-A

78002857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117584263-A-G

78002919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117584324-G-T

http://identifiers.org/hco/17/GRCh38#78003016-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#117584553-A-C

78003068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117584603-A-G

78003068-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117584603-A-T

78003198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117584694-A-G

78004297-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117591677-C-G

78004316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117591688-T-C

78004324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117591696-A-G

78004348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117591720-G-A

78004348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117591720-G-T

http://identifiers.org/hco/17/GRCh38#78004362-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#117591734-A-C

78004493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117591881-G-A

78005105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117593268-T-C

http://identifiers.org/hco/17/GRCh38#78005136-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#117593299-C-A

78006035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117593513-A-G

78006171-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117593849-G-C

78006234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117593925-T-C

78006390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117594050-T-C

http://identifiers.org/hco/17/GRCh38#78006392-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#117594052-A-C

http://identifiers.org/hco/17/GRCh38#78008383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#117595795-C-A

78008469-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117595869-T-A

78008526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117595924-A-G

78008800-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117596073-T-A

78008836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117596153-T-C

78011901-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117598126-C-G

78012004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 117598218-T-C

78012176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117598352-C-T

78013611-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117598828-C-G

78013862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117599089-G-A

78014179-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117599367-G-C

http://identifiers.org/hco/17/GRCh38#78014257-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#117599429-A-C

78014305-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117599461-T-A

78014305-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117599461-T-G

http://identifiers.org/hco/17/GRCh38#78014346-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#117599492-A-C

78014346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117599492-A-G

http://identifiers.org/hco/17/GRCh38#78014608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#117599612-C-A

78014608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117599612-C-T

78014627-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117599631-C-G

78014627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117599631-C-T

78014703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117599717-C-T

78019610-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117600411-C-G

78021196-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117601928-G-C

78021358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117602049-C-T

78021496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117602143-G-A

78022226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117602520-G-A

78022371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117602629-A-G

78027832-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117603855-A-T

78027921-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117603948-T-G

78031598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 117605034-C-T

78031854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117605290-A-G

http://identifiers.org/hco/17/GRCh38#78033548-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#117605405-A-C

78033716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117605589-A-G

78033749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117605621-T-C

78033749-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117605621-T-G

78033813-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117605686-C-G

78033937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117605793-A-G

78039641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117606531-G-A

78040255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117607014-G-A

78040331-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117607479-T-G

78040349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117607495-A-G

78040533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117607660-A-G

78040576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117607698-A-G

78040670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117607781-G-A

78040739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117607857-G-A

78041197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, undefined
orthologous variants: 117608034-G-T

http://identifiers.org/hco/17/GRCh38#78041263-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#117608063-A-C

78041491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117608200-A-G

78041626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117608327-A-G

78041893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117609040-A-G

78041921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117609065-T-C

78041960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117609088-A-G

78041985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117609112-A-G

78042172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117609654-C-T

78042223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117609704-G-A

78042243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117609724-C-T

78042368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117609820-A-G

http://identifiers.org/hco/17/GRCh38#78048748-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#117611672-A-C

78048856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 117611787-A-G

78048919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 117611850-G-T

78048990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 117611921-A-G

78048990-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 117611921-A-T

78049197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 117612128-T-C

78049284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, missense_variant
orthologous variants: 117612215-G-T

78049296-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, missense_variant
orthologous variants: 117612227-T-G

78049310-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, missense_variant
orthologous variants: 117612241-G-C

78049501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, missense_variant
orthologous variants: 117612432-A-G

78049582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, missense_variant
orthologous variants: 117612513-G-A

78049821-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 117612752-A-T

http://identifiers.org/hco/17/GRCh38#78050705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#117613636-C-A

78050705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, missense_variant
orthologous variants: 117613636-C-T

78050847-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 117613778-A-T

78056894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117619446-A-G

78057226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117619735-A-G

78057237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117619746-A-G

78057237-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117619746-A-T

http://identifiers.org/hco/17/GRCh38#78057650-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#117620026-A-C

78057806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117620122-T-C

78058018-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117620322-T-G

78058344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117620613-A-G

78058346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117620615-A-G

78058402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117620668-A-G

http://identifiers.org/hco/17/GRCh38#78058974-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#117621328-A-C

78059184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117621466-C-T

78059507-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117621715-T-G

78061314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117622030-A-G

78061834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117622300-T-C

78061996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117622447-A-G

78062343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117622713-T-C

78064958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117623219-G-T

78067458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117624196-C-T

78067592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117624314-T-C

78067686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117624366-T-C

78067944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117624625-G-A

78067967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117624634-G-A

78068011-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117624674-T-G

78069831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117625292-C-T

78070032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117625457-A-G

78070114-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117625535-C-G

http://identifiers.org/hco/17/GRCh38#78070189-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#117625606-A-C

http://identifiers.org/hco/17/GRCh38#78070232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#117625648-C-A

78070653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117626184-C-T

78070748-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117626262-G-C

78070904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117626459-T-C

http://identifiers.org/hco/17/GRCh38#78070918-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#117626473-C-A

78071013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117626682-G-A

78071013-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117626682-G-C

78071037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117626753-A-G

78071056-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117626771-A-T

78071132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 117626845-G-A

78071132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 117626845-G-T

78071356-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117627025-C-G

78072393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117628331-A-G

http://identifiers.org/hco/17/GRCh38#78072926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#117628998-C-A

78072926-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117628998-C-G

78072926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117628998-C-T

78073016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117629094-A-G

78073042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 117629122-G-A

78073042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 117629122-G-T

78073146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117629221-T-C

78073157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117629232-A-G

78073171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117629246-A-G

78073174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117629249-G-A

78073174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117629249-G-T

78073225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117629288-G-A

78073225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117629288-G-T

78073326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117629398-C-T

78074069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117629938-C-T

78074183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117630036-A-G

78074183-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117630036-A-T

78074350-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117630211-C-G

78074530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117630282-G-A

http://identifiers.org/hco/17/GRCh38#78074615-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#117630320-A-C

78074773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117630464-A-G

78074809-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117630502-A-T

78074811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117630504-G-A

http://identifiers.org/hco/17/GRCh38#78075444-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#117630989-A-C

78075486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117631031-G-A

78075486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117631031-G-T

http://identifiers.org/hco/17/GRCh38#78075700-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#117631379-A-C

78075700-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117631379-A-T

78075730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117631397-T-C

78075880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117631546-A-G

78076531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117631915-A-G

78076551-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117631942-T-A

78076763-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117632122-A-T

78076800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117632146-A-G

78076800-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117632146-A-T

78076801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117632147-T-C

78077514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117632827-A-G

78079320-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117633693-T-A

78079545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117633894-A-G

78080558-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117636288-A-T

78080816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117636520-A-G

78080839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117636543-T-C

78080858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117636562-A-G

78081070-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117636697-C-G

78081901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: -G-A

78081945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: -C-T

78082952-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117637908-A-T

78082998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117637956-C-T

78083011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117637969-G-T

http://identifiers.org/hco/17/GRCh38#78083186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#117638143-C-A

78083539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117638320-C-T

78083559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117638339-G-A

http://identifiers.org/hco/17/GRCh38#78083670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#117638448-C-A

78083773-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117638552-C-G

78083773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117638552-C-T

78083912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117638686-C-T

78086478-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117640049-T-A

78086478-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117640049-T-G

http://identifiers.org/hco/17/GRCh38#78086622-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#117640189-A-C

78086622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117640189-A-G

78086708-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117640272-T-A

78086722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117640282-A-G

78086803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117640345-A-G

78086830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117640372-G-A

78086833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117640375-C-T

78086939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: synonymous variant
orthologous variants: 117640489-A-G

78086948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: synonymous variant
orthologous variants: 117640498-G-A

78086948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: synonymous variant
orthologous variants: 117640498-G-T

78086990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: synonymous variant
orthologous variants: 117640540-G-A

78087066-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: missense variant
orthologous variants: 117640616-C-G

78087100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 117640650-G-T

78087131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117640679-G-A

78087133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117640681-G-T

78087138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117640686-T-C

78087193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117640728-G-A

78087219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117640750-G-T

78087635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117641150-A-G

78088029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117641404-T-C

78091345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117643721-G-A

78091345-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117643721-G-C

78091345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117643721-G-T

http://identifiers.org/hco/17/GRCh38#78091346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#117643722-C-A

78091346-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117643722-C-G

78091346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117643722-C-T

http://identifiers.org/hco/17/GRCh38#78091351-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#117643727-A-C

78091351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117643727-A-G

78091351-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117643727-A-T

http://identifiers.org/hco/17/GRCh38#78091371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#117643749-C-A

http://identifiers.org/hco/17/GRCh38#78091422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#117643785-C-A

78091422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117643785-C-T

http://identifiers.org/hco/17/GRCh38#78091619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#117643982-C-A

78091619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117643982-C-T

78091703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117644075-A-G

78091714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117644086-A-G

http://identifiers.org/hco/17/GRCh38#78092354-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#117644818-A-C

78092354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117644818-A-G

78092379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117644839-C-T

78092408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117644868-G-A

78092925-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 117646149-C-G

http://identifiers.org/hco/17/GRCh38#78092956-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#117646180-A-C

http://identifiers.org/hco/17/GRCh38#78093027-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#117646251-A-C

78093027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 117646251-A-G

78093182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117646402-G-A

78093182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117646402-G-T

78093191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117646411-G-A

78093191-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117646411-G-C

78093200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117646421-G-T

78093213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117646433-A-G

78093291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117646497-G-T

78093297-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117646503-G-C

78093297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117646503-G-T

http://identifiers.org/hco/17/GRCh38#78093333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#117646538-C-A

78093333-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117646538-C-G

78093333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117646538-C-T

78093387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117646599-T-C

78093570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117646742-A-G

78093585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117646757-T-C

78093596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117646764-T-C

78093774-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117646944-T-A

78094014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117647143-C-T

78094080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117647198-A-G

78094127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117647242-G-A

http://identifiers.org/hco/17/GRCh38#78098305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#117648728-C-A

http://identifiers.org/hco/17/GRCh38#78102400-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#117649677-A-C

78102400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117649677-A-G

78102415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117649692-G-A

http://identifiers.org/hco/17/GRCh38#78102428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#117649704-C-A

78102428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117649704-C-T

78102487-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 117649743-C-G

http://identifiers.org/hco/17/GRCh38#78102604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#117649890-C-A

78102604-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117649890-C-G

78102604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117649890-C-T

78102645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117649956-G-A

78102645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117649956-G-T

78102651-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117649962-T-A

78102651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117649962-T-C

78102651-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117649962-T-G

78102659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117649975-G-A

78102659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117649975-G-T

78102707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117650019-G-A

78102707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117650019-G-T

http://identifiers.org/hco/17/GRCh38#78102717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#117650029-C-A

78102717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117650029-C-T

78102762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117650085-T-C

78102796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117650114-G-A

78102807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117650126-A-G

http://identifiers.org/hco/17/GRCh38#78103307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#117650361-C-A

78103307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117650361-C-T

78103446-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: missense variant
orthologous variants: 117650482-G-C

http://identifiers.org/hco/17/GRCh38#78103608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#117650642-C-A

78103608-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117650642-C-G

http://identifiers.org/hco/17/GRCh38#78103698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#117650721-C-A

78103698-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117650721-C-G

78103698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117650721-C-T

78104147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117651040-G-A

78104177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117651064-G-A

78104187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117651074-A-G

78104334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: intron variant
orthologous variants: 117651211-T-C

78104595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: missense variant
orthologous variants: 117651427-G-T

78104717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: missense variant
orthologous variants: 117651549-G-A

78104717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: missense variant
orthologous variants: 117651549-G-T

78104746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: synonymous variant
orthologous variants: 117651578-G-A

78104746-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: synonymous variant
orthologous variants: 117651578-G-C

78104746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: synonymous variant
orthologous variants: 117651578-G-T

http://identifiers.org/hco/17/GRCh38#78104767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#117651599-C-A

78104767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: synonymous variant
orthologous variants: 117651599-C-T

78104872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: 3 prime UTR variant
orthologous variants: 117651703-G-A

78104872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: 3 prime UTR variant
orthologous variants: 117651703-G-T

http://identifiers.org/hco/17/GRCh38#78105005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#117651814-C-A

78105027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: 3 prime UTR variant
orthologous variants: 117651836-G-A

78105027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: 3 prime UTR variant
orthologous variants: 117651836-G-T

78105313-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: 3 prime UTR variant
orthologous variants: 117652106-C-G

78105313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: 3 prime UTR variant
orthologous variants: 117652106-C-T

78105615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: 3 prime UTR variant
orthologous variants: 117652368-G-A

78105615-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: 3 prime UTR variant
orthologous variants: 117652368-G-T

78105643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: 3 prime UTR variant
orthologous variants: 117652386-G-T

78105693-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: 3 prime UTR variant
orthologous variants: 117652460-T-G

78106235-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: 3 prime UTR variant
orthologous variants: 117653082-A-T

78106340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: 3 prime UTR variant
orthologous variants: 117653202-G-A

78106419-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: 3 prime UTR variant
orthologous variants: 117653288-T-G

78106555-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: 3 prime UTR variant
orthologous variants: 117653418-T-A

78106555-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: 3 prime UTR variant
orthologous variants: 117653418-T-G

78106565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: 3 prime UTR variant
orthologous variants: 117653428-G-A

http://identifiers.org/hco/17/GRCh38#78106912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#117653771-C-A

78106995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: 3 prime UTR variant
orthologous variants: 117653845-A-G

78107546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117654327-G-A

78107686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117654457-A-G

78108323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117654939-A-G

78108331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117654947-G-A

78108331-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117654947-G-T

78108335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117654951-G-A

78108335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117654951-G-T

78108368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117654984-A-G

78108378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29318
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117654994-G-T