http://identifiers.org/hco/1/GRCh38#9588965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: missense_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#149822368-C-A

9588965-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: missense_variant, undefined
orthologous variants: 149822368-C-G

9588965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: missense_variant, undefined
orthologous variants: 149822368-C-T

9588993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: synonymous_variant, undefined
orthologous variants: 149822340-G-A

9588993-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: synonymous_variant, undefined
orthologous variants: 149822340-G-C

9588993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: synonymous_variant, undefined
orthologous variants: 149822340-G-T

9589049-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron_variant, undefined
orthologous variants: 149822284-T-A

9589049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron_variant, undefined
orthologous variants: 149822284-T-C

http://identifiers.org/hco/1/GRCh38#9589109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#149822233-C-A

9589109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149822233-C-T

http://identifiers.org/hco/1/GRCh38#9589124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#149822223-C-A

9589124-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149822223-C-G

9589124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149822223-C-T

9589212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149822139-G-A

http://identifiers.org/hco/1/GRCh38#9589719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#149821752-C-A

9589804-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149821684-C-G

http://identifiers.org/hco/1/GRCh38#9589805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#149821683-C-A

9589805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149821683-C-T

9589823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149821665-G-A

9589876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149821633-G-A

9590024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149821522-A-G

9590068-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149821481-A-T

9590122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149821437-G-A

9590186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149821390-C-T

http://identifiers.org/hco/1/GRCh38#9590257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#149821318-C-A

9590688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149820809-T-C

9590727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149820766-G-A

9590791-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149820719-T-G

9590806-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149820706-C-G

9590806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149820706-C-T

9590840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149820672-T-C

9590879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149820626-G-A

9591028-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149820469-T-G

http://identifiers.org/hco/1/GRCh38#9591135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#149820389-C-A

9591484-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149820093-C-G

9591541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149820072-C-T

9591673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149819958-T-C

9591844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149819791-G-T

9592035-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149819568-C-G

http://identifiers.org/hco/1/GRCh38#9592330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#149819314-C-A

9592805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149818974-A-G

9592819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149818959-G-A

9592849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149818932-A-G

9593259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149818603-A-G

9593658-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron_variant, undefined
orthologous variants: 149818264-G-C

9593724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron_variant, undefined
orthologous variants: 149818200-G-A

9593983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149817985-G-T

9594041-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron_variant, undefined
orthologous variants: 149817919-G-C

9594478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149817516-T-C

9594563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149817428-G-A

9595099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149816981-G-A

9595235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149816908-C-T

9595502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149816711-G-A

9595556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149816643-G-A

http://identifiers.org/hco/1/GRCh38#9595580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#149816620-C-A

9595580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149816620-C-T

9595652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149816576-G-A

9595662-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149816572-C-G

9595749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149816508-G-A

9595749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149816508-G-T

http://identifiers.org/hco/1/GRCh38#9595783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#149816490-C-A

9595783-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149816490-C-G

9595792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149816481-G-A

9595792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149816481-G-T

9595821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149816476-G-A

9595831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149816466-T-C

http://identifiers.org/hco/1/GRCh38#9595832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#149816465-C-A

9595832-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149816465-C-G

9595845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149816453-G-A

9595847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149816451-G-A

9595847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149816451-G-T

9595848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149816450-C-T

9595855-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149816443-C-G

9595862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149816436-G-A

9595862-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149816436-G-C

9595862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149816436-G-T

9595867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149816431-C-T

http://identifiers.org/hco/1/GRCh38#9596045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#149816263-C-A

9596045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149816263-C-T

9596158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149816233-G-T

9596241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149816157-G-A

9596264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149816136-A-G

9596435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149816013-C-T

9596630-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149815890-C-G

9596630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149815890-C-T

9596647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149815877-T-C

9596738-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149815789-G-C

9596738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149815789-G-T

http://identifiers.org/hco/1/GRCh38#9596782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#149815770-C-A

9596782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149815770-C-T

9596784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149815768-G-A

9596827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149815749-T-C

9597083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149815499-T-C

9597159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149815472-G-A

9597159-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149815472-G-C

9597159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149815472-G-T

9597192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149815469-G-A

9597192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149815469-G-T

9597338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149815381-C-T

9597419-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149815298-C-G

9598461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: missense variant
orthologous variants: 149814155-G-A

9598461-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: missense variant
orthologous variants: 149814155-G-C

9598650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149813976-G-A

9598650-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149813976-G-C

9598669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149813957-T-C

9598695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149813931-G-A

9598695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149813931-G-T

9600908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149812894-G-A

9600913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149812893-G-A

9600913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149812893-G-T

9600914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149812892-G-A

http://identifiers.org/hco/1/GRCh38#9601222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#149812586-C-A

9601256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: missense variant
orthologous variants: 149812552-G-A

9601256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: missense variant
orthologous variants: 149812552-G-T

http://identifiers.org/hco/1/GRCh38#9601293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#149812518-C-A

9601300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: missense variant
orthologous variants: 149812511-G-A

9601300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: missense variant
orthologous variants: 149812511-G-T

9601500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149812314-T-C

9601939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149812022-G-A

http://identifiers.org/hco/1/GRCh38#9601942-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#149812019-C-A

9601942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149812019-C-T

9601978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149811976-G-T

9602000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149811963-G-A

9602000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149811963-G-T

9602067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: splice acceptor variant
orthologous variants: 149811887-A-G

9602322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 149811633-C-T

9602401-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 149811564-T-A

9602401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 149811564-T-C

9602401-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 149811564-T-G

http://identifiers.org/hco/1/GRCh38#9602403-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#149811562-C-A

9602403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 149811562-C-T

http://identifiers.org/hco/1/GRCh38#9602429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#149811536-C-A

9602452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 149811532-G-A

9602452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 149811532-G-T

9602502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 149811477-G-A

9602502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 149811477-G-T

http://identifiers.org/hco/1/GRCh38#9602738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#149811311-C-A

9602738-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 149811311-C-G

9602738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 149811311-C-T

9602826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 149811236-T-C

9602866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 149811187-T-C

9603010-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 149811081-T-A

9603010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 149811081-T-C

9603031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 149811060-G-A

9603031-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 149811060-G-C

9603031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 149811060-G-T

9603152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 149810899-G-A

9603152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 149810899-G-T

9603276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 149810775-T-C

http://identifiers.org/hco/1/GRCh38#9603337-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#149810713-C-A

9603337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 149810713-C-T

9603420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 149810654-C-T

http://identifiers.org/hco/1/GRCh38#9603488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#149810590-C-A

9603488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 149810590-C-T

9603504-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 149810569-G-C

9603504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 149810569-G-T

9603516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 149810558-G-A

9603516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 149810558-G-T

http://identifiers.org/hco/1/GRCh38#9603561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#149810525-C-A

9603561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 149810525-C-T

9603676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 149810412-A-G

9603718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 149810379-G-A

9603718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 149810379-G-T

9603724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 149810368-C-T

9603794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 149810294-G-A

http://identifiers.org/hco/1/GRCh38#9603802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#149810286-C-A

9603802-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 149810286-C-G

9603802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 149810286-C-T

9604292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 149809878-C-T

9604512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 149809688-G-T

9604601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 149809647-G-T

http://identifiers.org/hco/1/GRCh38#9604661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#149809591-C-A

9604661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 149809591-C-T

9604708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 149809541-C-T

9604802-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 149809470-T-A

9604802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 149809470-T-C

9605024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149809250-G-A

9605024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149809250-G-T

9605064-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149809224-G-C

9605064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149809224-G-T

9605071-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149809217-G-C

9605071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149809217-G-T

9605076-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149809212-A-T

9605083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149809205-A-G

http://identifiers.org/hco/1/GRCh38#9605090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#149809198-C-A

9605096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149809192-G-A

9605096-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149809192-G-T

9605102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149809189-G-A

9605102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149809189-G-T

9605184-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149809142-T-G

9605200-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149809127-G-C

9605201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149809126-C-T

9605250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149809085-G-A

9605653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149808838-C-T

9605966-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149808552-T-G

http://identifiers.org/hco/1/GRCh38#9606152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#149808277-C-A

9606152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron variant
orthologous variants: 149808277-C-T

9606319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 149808017-C-T

http://identifiers.org/hco/1/GRCh38#9606328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#149808007-C-A

9606328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 149808007-C-T

9606422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 149807924-G-A

9606422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 149807924-G-T

9606575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 149807783-G-A

9606756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149807603-G-A

9606756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149807603-G-T

9606847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149807514-G-T

9606922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149807441-C-T

9607200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149807245-C-T

9607416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149807034-T-C

9607416-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149807034-T-G

9607441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149807009-A-G

9607441-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149807009-A-T

9607480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149806974-G-T

9607564-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 149806887-C-G

9607564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 149806887-C-T

9607814-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 149806639-G-C

9607814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 149806639-G-T

9607815-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 149806638-A-T

9607819-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 149806634-T-A

9609698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 149804155-A-G

9609783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 149804092-G-T

9609804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 149804071-A-G

9609958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 149803915-C-T

9610042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 149803835-G-A

9610048-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 149803829-T-A

9610048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 149803829-T-C

9610231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 149803671-G-A

9610357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 149803579-T-C

http://identifiers.org/hco/1/GRCh38#9610372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#149803565-C-A

9610372-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 149803565-C-G

9610372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 149803565-C-T

9610386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 149803551-T-C

9610406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 149803533-T-C

9610406-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 149803533-T-G

http://identifiers.org/hco/1/GRCh38#9610423-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#149803519-A-C

9610423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 149803519-A-G

9610423-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 149803519-A-T

http://identifiers.org/hco/1/GRCh38#9610447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#149803490-C-A

9610447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 149803490-C-T

9610475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 149803445-A-G

9610634-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 149803271-C-G

9610634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 149803271-C-T

9610717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 149803191-G-A

9610769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 149803142-C-T

http://identifiers.org/hco/1/GRCh38#9610800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#149803111-C-A

9610800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 149803111-C-T

9611812-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 149802553-G-C

9611901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 149802464-T-C

9611901-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 149802464-T-G

9612081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 149802403-G-A

9612480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 149802079-C-T

9612732-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 149801741-C-G

9612732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 149801741-C-T

9612743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 149801730-A-G

http://identifiers.org/hco/1/GRCh38#9612938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#149801574-C-A

9612938-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 149801574-C-G

9612938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 149801574-C-T

http://identifiers.org/hco/1/GRCh38#9613134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#149801389-C-A

9613134-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 149801389-C-G

9613134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 149801389-C-T

http://identifiers.org/hco/1/GRCh38#9613176-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#149801348-C-A

9613340-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3 prime UTR variant
orthologous variants: 149801253-G-C

9613340-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3 prime UTR variant
orthologous variants: 149801253-G-T

http://identifiers.org/hco/1/GRCh38#9613428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#149801196-C-A

http://identifiers.org/hco/1/GRCh38#9613474-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#149801159-C-A

9613497-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3 prime UTR variant
orthologous variants: 149801154-T-G

9613617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3 prime UTR variant
orthologous variants: 149801032-G-T

http://identifiers.org/hco/1/GRCh38#9613622-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#149801030-A-C

9613622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3 prime UTR variant
orthologous variants: 149801030-A-G

9613622-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3 prime UTR variant
orthologous variants: 149801030-A-T

http://identifiers.org/hco/1/GRCh38#9613776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#149800874-C-A

http://identifiers.org/hco/1/GRCh38#9613790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#149800859-C-A

9613790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3 prime UTR variant
orthologous variants: 149800859-C-T

9613795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3 prime UTR variant
orthologous variants: 149800853-T-C

http://identifiers.org/hco/1/GRCh38#9613803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#149800845-C-A

9613803-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3 prime UTR variant
orthologous variants: 149800845-C-G

9613818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3 prime UTR variant
orthologous variants: 149800830-C-T

9613859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3 prime UTR variant
orthologous variants: 149800792-A-G

9613976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3 prime UTR variant
orthologous variants: 149800697-G-A

9614004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3 prime UTR variant
orthologous variants: 149800668-T-C

9614042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3 prime UTR variant
orthologous variants: 149800595-C-T

http://identifiers.org/hco/1/GRCh38#9614122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#149800509-C-A

9614122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3 prime UTR variant
orthologous variants: 149800509-C-T

9614176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3 prime UTR variant
orthologous variants: 149800449-T-C

9614332-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3 prime UTR variant
orthologous variants: 149800300-C-G

http://identifiers.org/hco/1/GRCh38#9614335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#149800297-C-A

9614464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3 prime UTR variant
orthologous variants: 149800181-T-C

http://identifiers.org/hco/1/GRCh38#9614523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#149800147-C-A

9614523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33719
most severe consequence: 3 prime UTR variant
orthologous variants: 149800147-C-T