92827086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37522054-A-G

92830941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron_variant, undefined
orthologous variants: 37523437-C-T

92831006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37523505-G-A

92831142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 37523671-G-A

http://identifiers.org/hco/10/GRCh38#92831185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37523710-C-A

92831185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 37523710-C-T

92831233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 37523757-G-A

92831243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 37523767-G-A

92831980-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37524230-T-A

92832085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37524322-T-C

92832117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37524348-T-C

92834215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37524754-A-G

92834626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 37525153-G-A

92834626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 37525153-G-T

92834627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 37525154-A-G

http://identifiers.org/hco/10/GRCh38#92834633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37525160-C-A

92834633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 37525160-C-T

92834666-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 37525190-T-G

92834670-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 37525194-T-A

92834670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 37525194-T-C

92834677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 37525201-T-C

92834689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 37525214-T-C

92834699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 37525222-T-C

92834712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 5_prime_UTR_variant, splice_acceptor_variant
orthologous variants: 37525235-G-A

http://identifiers.org/hco/10/GRCh38#92834839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37525362-C-A

92834839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37525362-C-T

92834975-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37525893-T-A

92835215-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37526149-G-C

92837698-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37527172-T-G

92837708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37527182-A-G

92839440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37528453-A-G

http://identifiers.org/hco/10/GRCh38#92840136-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37529116-A-C

92840146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37529126-G-T

92840380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37529331-T-C

92841439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37531411-T-C

http://identifiers.org/hco/10/GRCh38#92841516-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37531487-A-C

92844267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37533187-G-A

92844382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37533295-A-G

92844631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37533565-A-G

92844709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37533643-A-G

92844807-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37533749-A-T

92844911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37533854-C-T

92844958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37533901-T-C

92844994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37533937-G-A

92845104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37534043-G-A

92846328-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37535627-C-G

http://identifiers.org/hco/10/GRCh38#92846372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37535678-C-A

92847065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37537525-G-A

92847114-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37537571-C-G

92847276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37537698-G-A

92847298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron_variant, undefined
orthologous variants: 37537721-G-T

92847530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37537979-C-T

http://identifiers.org/hco/10/GRCh38#92847548-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37537997-C-A

http://identifiers.org/hco/10/GRCh38#92847790-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37538238-A-C

http://identifiers.org/hco/10/GRCh38#92847825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37538274-C-A

92847825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37538274-C-T

92847863-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37538295-T-G

92847956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37538384-G-T

92848124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37538532-C-T

http://identifiers.org/hco/10/GRCh38#92848310-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#37538690-A-C

92848310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron_variant, undefined
orthologous variants: 37538690-A-G

92848310-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron_variant, undefined
orthologous variants: 37538690-A-T

92848318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37538698-G-A

92848318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37538698-G-T

http://identifiers.org/hco/10/GRCh38#92848434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37538813-C-A

92848434-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37538813-C-G

http://identifiers.org/hco/10/GRCh38#92848439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37538818-C-A

92848439-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37538818-C-G

92848439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37538818-C-T

92848494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 37538873-G-A

92848494-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 37538873-G-C

92848494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 37538873-G-T

92848556-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 37538935-T-A

92848556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 37538935-T-C

92848556-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 37538935-T-G

92848655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37539034-G-A

92848655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37539034-G-T

http://identifiers.org/hco/10/GRCh38#92848667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37539043-C-A

92848667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37539043-C-T

http://identifiers.org/hco/10/GRCh38#92848669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37539045-C-A

92848669-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37539045-C-G

92848669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37539045-C-T

92848708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron_variant, undefined
orthologous variants: 37539083-T-C

92848802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37539158-G-T

92849068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron_variant, undefined
orthologous variants: 37539339-T-C

92849203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37539472-G-T

92849421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37539637-C-T

92849563-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37539752-A-T

92849565-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37539754-G-C

92849700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron_variant, undefined
orthologous variants: 37539882-T-C

92849701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron_variant, undefined
orthologous variants: 37539883-G-T

92849883-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37540062-C-G

92868148-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37546239-G-C

92868567-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37546671-C-G

http://identifiers.org/hco/10/GRCh38#92868651-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37546769-A-C

92868680-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37546798-T-G

92872838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37549764-T-C

92872912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 37549838-A-G

92873072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 37550001-A-G

92873127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 37550054-T-C

92873690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37551059-G-A

92874155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37551190-G-A

92874170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37551205-A-G

92874183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37551220-C-T

92874293-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37551324-T-A

92879591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37551752-G-T

92879836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37551990-G-T

92880485-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37552414-C-G

92880720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37552601-C-T

92880730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37552609-C-T

92882625-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37552797-T-A

92882625-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37552797-T-G

92882627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37552799-T-C

92882697-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37552887-T-G

92883778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37553331-G-A

92884806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37554222-A-G

92885256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37554602-C-T

92885292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37554637-C-T

92885907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37555063-A-G

92885907-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37555063-A-T

92886145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37555425-A-G

92886232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37555506-A-G

92886252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37555531-A-G

92886308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37555575-G-A

92886332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37555597-C-T

92886449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37555708-C-T

92886461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37555720-A-G

92886963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37556034-T-C

92891135-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37556996-T-G

92891206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37557061-G-A

92891401-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37557244-C-G

92891790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37557452-C-T

92891863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37557520-C-T

92891871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37557528-A-G

92891879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37557535-G-A

92891989-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37557643-A-T

92892303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron_variant, undefined
orthologous variants: 37557911-G-A

92892423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron_variant, undefined
orthologous variants: 37557999-T-C

92892471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron_variant, undefined
orthologous variants: 37558048-A-G

92892598-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron_variant, undefined
orthologous variants: 37558149-T-A

92892598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron_variant, undefined
orthologous variants: 37558149-T-C

92892955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37558449-T-C

92892973-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37558465-C-G

92893077-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37558552-T-A

92893098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37558573-G-A

92893144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37558618-C-T

92893146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37558620-A-G

92893201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37558675-T-C

92893252-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37558729-T-A

92893502-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: synonymous variant
orthologous variants: 37558984-T-A

92893502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: synonymous variant
orthologous variants: 37558984-T-C

92893539-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37559021-T-G

92893835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37559151-A-G

92893982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37559258-C-T

92894237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37559488-C-T

92894610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37559859-G-A

92894786-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 37560033-T-A

92894857-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37560186-T-G

92894861-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37560190-C-G

92894865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37560194-G-A

92894865-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37560194-G-C

92894865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37560194-G-T

92895060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37560436-A-G

92895140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37560514-G-T

92895146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37560520-G-T

92895163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37560536-A-G

92895317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37560689-C-T

92896907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37561246-T-C

92896936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37561275-G-A

92897209-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37561510-T-G

92897273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37561537-C-T

92899182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37561850-T-C

92899579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37562142-T-C

http://identifiers.org/hco/10/GRCh38#92899596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37562157-C-A

92899596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 37562157-C-T

92899651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 3_prime_UTR_variant, intron_variant, splice_region_variant
orthologous variants: 37562212-T-C

92899651-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 3_prime_UTR_variant, intron_variant, splice_region_variant
orthologous variants: 37562212-T-G

http://identifiers.org/hco/10/GRCh38#92899699-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37562258-A-C

92899699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37562258-A-G

92899700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37562259-G-A

http://identifiers.org/hco/10/GRCh38#92899703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37562262-C-A

92899703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37562262-C-T

92899826-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37562375-A-T

92899835-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37562384-T-A

92899835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37562384-T-C

92899855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37562404-G-A

http://identifiers.org/hco/10/GRCh38#92899886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37562440-C-A

92899886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37562440-C-T

http://identifiers.org/hco/10/GRCh38#92899895-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37562448-A-C

92899895-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37562448-A-T

92899965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37562516-A-G

92899979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37562533-G-T

92899984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37562538-T-C

92899997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37562551-G-A

92899997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37562551-G-T

http://identifiers.org/hco/10/GRCh38#92900348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37562715-C-A

92900362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37562729-G-T

92900401-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37562762-T-A

92900490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37562836-A-G

http://identifiers.org/hco/10/GRCh38#92900532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37562881-C-A

92900721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37563056-G-A

http://identifiers.org/hco/10/GRCh38#92900867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37563213-C-A

92900867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37563213-C-T

http://identifiers.org/hco/10/GRCh38#92900944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37563293-C-A

92908651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37564631-G-T

92909384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37565345-G-T

92909399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37565360-T-C

92909682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37565620-G-A

92909682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37565620-G-T

92909761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37565681-A-G

92909819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37565740-A-G

http://identifiers.org/hco/10/GRCh38#92915747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37566857-C-A

92915747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37566857-C-T

http://identifiers.org/hco/10/GRCh38#92915750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37566860-C-A

92915750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 37566860-C-T

92915823-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 37566933-T-A

92915823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 37566933-T-C

92915825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 37566935-T-C

92915874-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 37566984-G-C

92915874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 37566984-G-T

92915880-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 37566990-T-A

92915880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 37566990-T-C

http://identifiers.org/hco/10/GRCh38#92919062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37569697-C-A

92919290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37569905-T-C

92919668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37570275-G-A

92919709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37570316-A-G

92919843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37570520-G-A

92919843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37570520-G-T

92919878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37570551-A-G

92919878-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37570551-A-T

92919926-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37570596-T-A

92920002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 37570661-T-C

92920017-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 37570676-T-A

92926937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37573257-T-C

92927049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37573369-T-C

92927245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37573556-A-G

92927256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37573569-C-T

http://identifiers.org/hco/10/GRCh38#92927789-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37573741-A-C

92927858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37573810-T-C

92927917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37573850-T-C

92927951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37573861-G-T

92927974-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37573884-C-G

92927974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37573884-C-T

92928222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37574123-T-C

92928294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37574215-G-A

92928295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37574216-T-C

92928318-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: intron variant
orthologous variants: 37574239-A-T

92928346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: missense variant
orthologous variants: 37574266-A-G

http://identifiers.org/hco/10/GRCh38#92928410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37574330-C-A

92928410-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 37574330-C-G

92928441-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37574361-G-C

92928471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37574383-T-C

92928472-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37574384-T-A

92928593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37574504-A-G

http://identifiers.org/hco/10/GRCh38#92928608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37574519-C-A

92929096-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37575166-C-G

92929111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37575181-A-G

http://identifiers.org/hco/10/GRCh38#92934008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37575958-C-A

92934008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37575958-C-T

http://identifiers.org/hco/10/GRCh38#92934037-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37575986-A-C

92934037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37575986-A-G

92934037-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37575986-A-T

92934061-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37576010-T-A

92934223-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37576166-A-T

92934224-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37576167-T-A

92934267-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37576213-G-C

92934267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37576213-G-T

92934302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 37576258-G-T

92934513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37576448-G-A

92934513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37576448-G-T

92934596-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37576531-T-A

http://identifiers.org/hco/10/GRCh38#92934735-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37576670-A-C

http://identifiers.org/hco/10/GRCh38#92935081-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37576946-A-C

92935119-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37576977-C-G

92935181-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37577047-A-T

92935307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37577252-A-G

92935582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37578094-T-C

92935607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37578121-A-G

92935611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37578151-G-A

92935669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37578205-A-G

http://identifiers.org/hco/10/GRCh38#92935676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37578212-C-A

92935676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37578212-C-T

92935684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37578220-A-G

92935717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37578234-A-G

92935752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37578262-A-G

92935800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37578285-G-A

92935800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37578285-G-T

http://identifiers.org/hco/10/GRCh38#92935897-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37578382-C-A

92935897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37578382-C-T

92935906-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37578395-T-G

92935918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37578411-T-C

92935919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37578412-G-A

92935919-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37578412-G-C

92935919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37578412-G-T

http://identifiers.org/hco/10/GRCh38#92936007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37578474-C-A

92936007-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37578474-C-G

92936027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37578492-A-G

http://identifiers.org/hco/10/GRCh38#92936059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37578518-C-A

92937619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37578609-G-A

92938018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37578909-T-C

http://identifiers.org/hco/10/GRCh38#92940909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37579499-C-A

92940909-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37579499-C-G

92940909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37579499-C-T

92940912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37579502-A-G

92940922-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37579513-T-G

92941022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37579591-A-G

92941195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37579752-C-T

92941400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37580039-C-T

92942023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37580667-A-G

http://identifiers.org/hco/10/GRCh38#92948097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37581914-C-A

92948097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37581914-C-T

92948104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37581921-G-T

92948120-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37581937-A-T

92948121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37581938-T-C

92948138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37581951-G-A

92948138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37581951-G-T

92948142-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37581955-C-G

92948178-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37582015-G-T

92948207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37582050-T-C

92948211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37582054-G-A

92948211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37582054-G-T

92948231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37582074-T-C

92948315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 37582151-T-C

http://identifiers.org/hco/10/GRCh38#92948355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37582191-C-A

92948386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 37582222-G-A

92948386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 37582222-G-T

http://identifiers.org/hco/10/GRCh38#92948438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37582270-C-A

92948438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37582270-C-T

92948550-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37582397-G-T

92948712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37582516-T-C

92951376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37584051-A-G

92951514-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37584182-A-T

92951579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37584246-A-G

92951605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37584272-T-C

92951627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37584297-G-T

92951904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37584868-C-T

92951977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37584927-A-G

92952308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 37585578-A-G

92954357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37586692-C-T

92954412-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37586743-T-G

92954480-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37586804-A-T

92954526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37586915-A-G

http://identifiers.org/hco/10/GRCh38#92954578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37586966-C-A

http://identifiers.org/hco/10/GRCh38#92954589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37586977-C-A

92954589-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37586977-C-G

92954617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37587001-T-C

92954770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37587148-T-C

92955381-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37587818-T-A

92955452-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37587877-G-C

92955452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37587877-G-T

92955474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37587899-T-C

92955474-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37587899-T-G

92955516-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37587946-A-T

http://identifiers.org/hco/10/GRCh38#92955764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37588189-C-A

92955764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37588189-C-T

92955783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37588206-G-A

92955783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37588206-G-T

92955785-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37588208-T-A

http://identifiers.org/hco/10/GRCh38#92955805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37588213-C-A

92955922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37588312-C-T

92956283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37588653-T-C

92964383-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37589762-T-A

92964816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37590513-T-C

92964941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37590619-T-C

92965208-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37590841-C-G

92965208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37590841-C-T

92965297-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37590914-G-C

http://identifiers.org/hco/10/GRCh38#92965351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#37590986-C-A

92965369-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37590997-A-T

92965388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37591016-T-C

92965789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37591137-A-G

92965798-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37591139-G-C

92965841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37591183-A-G

92965938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37591256-A-G

92966194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37591471-C-T

92966251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37591547-C-T

92967331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37591737-T-C

92967356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37591763-C-T

http://identifiers.org/hco/10/GRCh38#92967370-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37591777-A-C

92967370-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37591777-A-T

http://identifiers.org/hco/10/GRCh38#92967679-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37592625-A-C

92967679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37592625-A-G

http://identifiers.org/hco/10/GRCh38#92967690-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37592636-A-C

http://identifiers.org/hco/10/GRCh38#92968075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37592989-C-A

92968075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37592989-C-T

92968969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37593235-G-A

92969031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37593300-G-A

92969064-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37593330-A-T

92969081-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37593352-A-T

92969298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37593622-C-T

92969299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37593623-G-A

92969382-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37593655-C-G

92969448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37593713-G-A

92969552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37593835-C-T

92969570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37593852-T-C

http://identifiers.org/hco/10/GRCh38#92973918-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37597242-C-A

92973918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37597242-C-T

http://identifiers.org/hco/10/GRCh38#92973928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37597252-C-A

92973928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37597252-C-T

http://identifiers.org/hco/10/GRCh38#92973953-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37597277-A-C

92974028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37597349-T-C

92974067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 37597388-A-G

92974359-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37597686-A-T

92974420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37597742-T-C

92976840-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37598162-T-A

92976840-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37598162-T-G

92976856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37598178-G-A

92985889-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37599852-C-G

92986006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37599876-T-C

92986014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37599889-A-G

92986310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37600325-A-G

92986425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37600434-C-T

92986590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37600548-G-A

92986622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37600581-G-A

92986622-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37600581-G-C

92986663-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37600661-T-A

92986698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37600745-G-A

92986698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37600745-G-T

92986913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37600941-A-G

http://identifiers.org/hco/10/GRCh38#92987000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37601017-C-A

92987000-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37601017-C-G

92987237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37601286-A-G

92987533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37601565-G-T

http://identifiers.org/hco/10/GRCh38#92987619-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37601657-A-C

92987623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37601661-A-G

92987857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37601899-C-T

http://identifiers.org/hco/10/GRCh38#92987862-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37601904-A-C

92988357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37617088-T-C

92989018-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37617386-T-G

92989109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37617473-A-G

http://identifiers.org/hco/10/GRCh38#92989112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37617476-C-A

92989231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37617583-G-T

92990349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37618681-T-C

92990384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37618716-G-T

92990423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37618754-A-G

92991093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37621874-T-C

92991568-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37622575-T-A

92991807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37622764-A-G

92993012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37623704-G-T

92993260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37624080-T-C

http://identifiers.org/hco/10/GRCh38#92993575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37624433-C-A

92993575-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37624433-C-G

92993834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37624682-C-T

92993901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37624749-A-G

92994493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37625351-T-C

92994750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37625582-A-G

92994782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37625608-T-C

92994852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37625686-A-G

92995488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37626280-G-A

92995536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37626328-T-C

92995635-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37626419-T-G

92995686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37626469-C-T

92995783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37626566-A-G

92996041-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37626833-C-G

92996291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37627083-G-T

92996400-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37627209-C-G

92996459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37627265-C-T

92996478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37627284-G-A

92996981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37627641-T-C

92997225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37627884-C-T

92997417-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37628018-T-A

92997455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37628051-G-T

92997618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37628214-A-G

92997652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37628248-G-T

http://identifiers.org/hco/10/GRCh38#92997657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37628253-C-A

92997657-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37628253-C-G

92997657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37628253-C-T

92997672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37628268-A-G

92997672-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37628268-A-T

92997745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37628333-T-C

92997745-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37628333-T-G

92997758-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37628346-T-A

92997811-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37628396-T-A

92998150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37629022-T-C

92998169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37629041-C-T

92998173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37629045-A-G

92998278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37629120-A-G

92998384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37629238-G-A

92998426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37629280-C-T

92998497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37629343-T-C

92999477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37629938-T-C

93000268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37630298-T-C

93000332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37631329-G-A

93000369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37631373-A-G

93000486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37631461-G-A

93000522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37631476-G-A

93000583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37631537-A-G

http://identifiers.org/hco/10/GRCh38#93000840-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37632008-A-C

93000981-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37632178-T-A

93000986-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37632183-C-G

93001454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37632649-C-T

93001510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37632701-A-G

93001631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37632757-C-T

93001824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37632963-C-T

93001948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37633025-A-G

93001951-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37633028-C-G

93004076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37633863-C-T

http://identifiers.org/hco/10/GRCh38#93004182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37633975-C-A

93004268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37634146-T-C

93004384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37634254-G-A

93004643-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37634516-T-G

93004852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37634704-C-T

93004875-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37634727-T-A

http://identifiers.org/hco/10/GRCh38#93005591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37635417-C-A

93005778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37635642-G-A

http://identifiers.org/hco/10/GRCh38#93006175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37636207-C-A

93006278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37636319-A-G

93006361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37636398-C-T

http://identifiers.org/hco/10/GRCh38#93006455-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37636478-A-C

93006492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37636517-A-G

93006493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37636518-T-C

93009274-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37637875-C-G

93009330-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37637931-A-T

93009411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37637996-G-A

93009733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37638298-G-A

93009797-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37638351-A-T

93009807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37638363-G-A

93010269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37638854-G-T

93010304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37638889-T-C

93010350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37638935-C-T

93010775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37639046-G-A

93011011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37639393-G-T

93011013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37639395-A-G

93013263-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37641249-T-A

93013263-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37641249-T-G

93013694-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37641355-T-A

93013731-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37641390-G-C

93013858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37641509-A-G

93013860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37641511-C-T

93014050-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37641702-T-A

93014086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37641734-G-A

93014086-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37641734-G-C

http://identifiers.org/hco/10/GRCh38#93014184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37641817-C-A

93014184-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37641817-C-G

93014184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37641817-C-T

93014191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 37641828-T-C

93014295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37641920-T-C

93014342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 37641966-T-C

http://identifiers.org/hco/10/GRCh38#93014377-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37641996-A-C

93014377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 37641996-A-G

93014964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37642496-C-T

93015005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37642536-G-A

93015095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37642613-A-G

93015187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37642704-G-T

93021526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37643161-G-A

93021604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37643225-T-C

93021690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37643310-T-C

http://identifiers.org/hco/10/GRCh38#93021942-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37643506-A-C

93022137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37643926-T-C

93022150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37643939-A-G

93022189-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37643975-T-G

93022377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37644158-G-A

93022429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37644209-A-G

93022438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37644216-C-T

93022451-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37644231-C-G

93022466-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37644246-G-C

93022476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37644253-C-T

93022632-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37644411-G-T

93022780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37644530-G-A

93023026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37644766-G-A

93023026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37644766-G-T

93023488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37645218-T-C

93023580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37645309-T-C

93023645-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37645364-G-C

93023807-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37645524-T-G

93023876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37645568-A-G

93024015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37645685-T-C

93024087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37645749-T-C

93024812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37646275-C-T

93024827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37646288-G-A

93030427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37648777-A-G

93030460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37648810-G-A

93030620-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37648964-T-G

93030716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37649029-T-C

93030803-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37649121-A-T

93030893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37649422-C-T

93030997-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37649546-A-T

93031010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37649567-G-A

93031109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37649668-A-G

93032602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37650550-G-A

93032795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37650764-A-G

93032917-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37650871-T-A

93033005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37650939-A-G

93033230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37651139-G-A

93033230-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37651139-G-C

93033484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37651356-G-A

93033657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37651589-C-T

93033714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37651710-T-C

93033787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37651962-A-G

93033815-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37652078-G-C

93033904-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37652143-A-T

93034037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37652265-A-G

93034164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37652365-G-T

93034267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37652464-A-G

93034436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37652602-A-G

93034689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37652859-A-G

93035026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37653192-G-A

http://identifiers.org/hco/10/GRCh38#93035394-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37653571-A-C

93035413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37653585-C-T

93036483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37654144-A-G

93036792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37654411-T-C

93036926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37654674-T-C

93036926-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37654674-T-G

93036961-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37654709-A-T

93036992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37654739-C-T

93042899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37659749-C-T

93042903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37659753-A-G

93042917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37659767-G-A

93043350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37659882-A-G

93043497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37660062-G-A

http://identifiers.org/hco/10/GRCh38#93043672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37660231-C-A

93043672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37660231-C-T

93044016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37660475-A-G

93044236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37660680-C-T

93044346-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37660755-A-T

93045119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37661476-G-A

93045120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37661477-C-T

http://identifiers.org/hco/10/GRCh38#93045236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37661650-C-A

93045279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37661693-A-G

93045521-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37661927-T-A

93051178-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37663511-A-T

93051181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37663514-G-A

93051290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37664108-T-C

93051304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37664119-C-T

93051358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37664182-G-A

93051571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37664378-G-A

93051638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37664459-T-C

93051643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37664464-C-T

93051705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37664601-A-G

93051738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37664633-T-C

http://identifiers.org/hco/10/GRCh38#93051751-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37664646-A-C

93052000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37664885-C-T

93052121-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37664996-C-G

http://identifiers.org/hco/10/GRCh38#93052126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37665001-C-A

93052225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37665080-T-C

93052481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37665321-T-C

93052822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37665650-A-G

93053037-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37665848-A-T

93053080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37665889-C-T

93053865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37666946-A-G

93053975-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37667049-C-G

93054424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37667455-A-G

93054484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37667505-G-A

93054544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37667557-A-G

93054544-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37667557-A-T

93056297-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37669545-T-G

93056698-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37669881-G-C

93056797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37669989-G-A

93056797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37669989-G-T

93057016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 37670200-A-G

http://identifiers.org/hco/10/GRCh38#93057169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37670426-C-A

93057465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37670733-T-C

http://identifiers.org/hco/10/GRCh38#93058116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37671164-C-A

93058116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37671164-C-T

93058126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37671173-G-A

93058126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37671173-G-T

http://identifiers.org/hco/10/GRCh38#93058144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37671191-C-A

http://identifiers.org/hco/10/GRCh38#93058149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37671196-C-A

93058149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37671196-C-T

93058150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37671197-A-G

93058160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37671207-A-G

93058191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37671264-T-C

http://identifiers.org/hco/10/GRCh38#93058424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37671469-C-A

http://identifiers.org/hco/10/GRCh38#93058452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37671497-C-A

93058458-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37671504-T-A

93058497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37671547-G-T

93058549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 3 prime UTR variant
orthologous variants: 37671599-A-G

93058549-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 3 prime UTR variant
orthologous variants: 37671599-A-T

http://identifiers.org/hco/10/GRCh38#93058563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37671611-C-A

93058563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 3 prime UTR variant
orthologous variants: 37671611-C-T

http://identifiers.org/hco/10/GRCh38#93058630-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37671678-A-C

93058630-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 3 prime UTR variant
orthologous variants: 37671678-A-T

http://identifiers.org/hco/10/GRCh38#93058926-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37671961-A-C

http://identifiers.org/hco/10/GRCh38#93059045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37672073-C-A

93059287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 3 prime UTR variant
orthologous variants: 37672301-G-T

93059359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 3 prime UTR variant
orthologous variants: 37672370-T-C

http://identifiers.org/hco/10/GRCh38#93059374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23196
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37672385-C-A