86878419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3 prime UTR variant
orthologous variants: 9531241-C-T

86878466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3 prime UTR variant
orthologous variants: 9531194-C-T

86878510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3 prime UTR variant
orthologous variants: 9531154-G-A

86878510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3 prime UTR variant
orthologous variants: 9531154-G-T

http://identifiers.org/hco/7/GRCh38#86878604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9531062-C-A

86878936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3 prime UTR variant
orthologous variants: 9530708-G-A

86878936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3 prime UTR variant
orthologous variants: 9530708-G-T

86879283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3 prime UTR variant
orthologous variants: 9530369-C-T

86879396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3 prime UTR variant
orthologous variants: 9530274-T-C

86879531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3 prime UTR variant
orthologous variants: 9530135-T-C

86879655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3 prime UTR variant
orthologous variants: 9530031-C-T

86880122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 9529557-A-G

http://identifiers.org/hco/7/GRCh38#86880301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9529381-C-A

86880481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 9529243-G-A

86880702-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9529030-C-G

86880702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9529030-C-T

86883063-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9527579-A-T

86883307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 9527361-C-T

86883496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 9527198-G-A

86883673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 9527046-G-T

86883723-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 9526997-G-C

86883864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 9526859-T-C

86884043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 9526537-A-G

86886423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 9518426-A-G

http://identifiers.org/hco/7/GRCh38#86886519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9518310-C-A

86886547-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 9518261-T-G

86886792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 9518104-C-T

86886901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 9518003-C-T

86887044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 9517955-A-G

86887109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 9517893-A-G

86887263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 9517746-G-A

86887263-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 9517746-G-C

http://identifiers.org/hco/7/GRCh38#86887408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9517507-C-A

86887422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 9517493-A-G

86887521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 9517337-T-C

86887527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 9517331-T-C

86887567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 9517302-G-T

86887619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 9517251-T-C

86887619-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 9517251-T-G

86887655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 9517217-G-A

86887784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 9517091-A-G

86887841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 9517044-C-T

86887973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 9517010-A-G

86888095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 9516988-G-A

86888150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 9516935-C-T

86888471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 9516685-G-T

86888495-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 9516668-C-G

86888495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 9516668-C-T

86888538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 9516625-G-A

86888626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 9516532-G-A

86888875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 9516314-T-C

86888968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 9516232-G-A

86888968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 9516232-G-T

86889040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 9516150-T-C

86889277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 9515863-T-C

86889277-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 9515863-T-G

86889828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 9515672-T-C

86889845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 9515656-A-G

86890071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 9515432-T-C

86890172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 9515333-C-T

86890219-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 9515298-T-A

86890219-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 9515298-T-G

86890362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 9515062-T-C

86890718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 9514772-T-C

86890736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 9514759-G-A

86890736-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 9514759-G-T

86890757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 9514738-C-T

86890805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 9514702-G-A

86890809-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 9514698-T-G

86890941-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 9514244-G-C

http://identifiers.org/hco/7/GRCh38#86890966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9514219-C-A

86891105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 9514077-C-T

http://identifiers.org/hco/7/GRCh38#86891381-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9513793-A-C

86891473-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9513286-A-T

http://identifiers.org/hco/7/GRCh38#86891544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9513200-C-A

http://identifiers.org/hco/7/GRCh38#86891597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9513148-C-A

86891597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9513148-C-T

86891919-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9512834-A-T

86891940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9512812-T-C

86891968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9512787-A-G

86891992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9512757-G-A

86891992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9512757-G-T

86892071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9512680-A-G

86892100-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9512650-C-G

86892100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9512650-C-T

86892122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9512628-C-T

86892443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9511934-G-A

86892457-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9511920-T-A

86892486-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9511891-A-T

86892623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9511785-C-T

86892726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9511694-T-C

86892737-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9511683-T-A

86892783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9511636-T-C

86892825-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9511593-G-C

86892825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9511593-G-T

http://identifiers.org/hco/7/GRCh38#86892937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9511483-C-A

86892937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, stop_gained
orthologous variants: 9511483-C-T

86892979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 9511441-G-T

86893015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 9511405-A-G

86893126-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9511294-T-A

86893126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9511294-T-C

86893126-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9511294-T-G

http://identifiers.org/hco/7/GRCh38#86893129-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9511291-A-C

86893136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9511284-G-A

86893136-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9511284-G-C

86893136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9511284-G-T

86893180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9511240-T-C

86893242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9511185-G-A

86893242-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9511185-G-C

86893295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9511128-A-G

86893305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9511119-G-T

86893377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9511079-G-A

86893413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9511048-A-G

86893418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9511043-G-A

86893583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9510937-G-A

http://identifiers.org/hco/7/GRCh38#86893888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9510660-C-A

86893888-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9510660-C-G

86893994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9510565-G-A

86894012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9510540-G-T

86894408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9510170-T-C

86894408-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9510170-T-G

86894497-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9510080-C-G

86894729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9509857-A-G

86894816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9509770-T-C

86894988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9509597-T-C

86895003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9509581-C-T

86895203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9509372-T-C

86897674-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9509152-T-G

86897682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9509143-C-T

http://identifiers.org/hco/7/GRCh38#86897781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9509043-C-A

86897781-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9509043-C-G

86897781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9509043-C-T

86897997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9508813-A-G

86898157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9508669-A-G

86898205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9508617-G-A

86898290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9508541-T-C

86898358-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9508484-G-C

http://identifiers.org/hco/7/GRCh38#86898445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9508399-C-A

86898447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9508397-G-A

86898447-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9508397-G-C

86899025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9507623-A-G

86899076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9507589-G-A

86899156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9507513-C-T

86899208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9507461-T-C

http://identifiers.org/hco/7/GRCh38#86899677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9504608-C-A

86899677-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9504608-C-G

86899677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9504608-C-T

86899678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9504607-C-T

http://identifiers.org/hco/7/GRCh38#86899989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9504304-C-A

86900253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9504041-T-C

86900754-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9503612-T-A

86903438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9501417-T-C

http://identifiers.org/hco/7/GRCh38#86903634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9501241-C-A

86903634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9501241-C-T

86903644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9501231-G-A

86903774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9501101-G-A

http://identifiers.org/hco/7/GRCh38#86903775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9501100-C-A

http://identifiers.org/hco/7/GRCh38#86903867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9501001-C-A

86903966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9500910-T-C

86904077-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9500787-C-G

http://identifiers.org/hco/7/GRCh38#86904146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9500719-C-A

86904316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9500576-G-A

86904396-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9500509-T-A

86904425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9500485-G-A

http://identifiers.org/hco/7/GRCh38#86904612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9500283-C-A

86904612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9500283-C-T

86904833-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9500082-T-A

86905308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 9499860-T-C

86905397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9499792-C-T

http://identifiers.org/hco/7/GRCh38#86905482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9499707-C-A

86905617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9499579-C-T

86905841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9499358-A-G

86906212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9499002-A-G

86906246-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9498972-C-G

http://identifiers.org/hco/7/GRCh38#86906389-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9498809-A-C

86906432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9498767-G-A

86906496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9498711-G-A

http://identifiers.org/hco/7/GRCh38#86906880-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9498521-A-C

86906880-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9498521-A-T

86907282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9498200-T-C

86907343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9498145-C-T

86907419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9498063-A-G

86907445-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9498037-G-C

86907450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9498032-A-G

86907564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9497929-G-A

86907564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9497929-G-T

86907605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9497891-A-G

86907606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9497890-T-C

86907610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9497886-A-G

http://identifiers.org/hco/7/GRCh38#86907822-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9497668-A-C

86907844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9497643-T-C

86907902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9497586-G-T

http://identifiers.org/hco/7/GRCh38#86907920-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9497569-C-A

86907944-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9497545-T-A

86907944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9497545-T-C

86908057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9497462-A-G

86908103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9497405-T-C

86908238-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9497176-T-A

86908372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9497038-A-G

http://identifiers.org/hco/7/GRCh38#86908495-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9496940-A-C

86908495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 9496940-A-G

86908495-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 9496940-A-T

86908638-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9496794-T-A

86908675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9496758-A-G

http://identifiers.org/hco/7/GRCh38#86908736-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9496704-C-A

86908883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9496552-A-G

86908934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9496516-C-T

86909165-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9496323-G-C

86909294-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9496230-C-G

86909390-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9496146-C-G

86909612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9495774-A-G

http://identifiers.org/hco/7/GRCh38#86909674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9495681-C-A

http://identifiers.org/hco/7/GRCh38#86909732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9495631-C-A

86909744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9495619-G-A

86909744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9495619-G-T

86909758-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9495605-A-T

86909849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 9495514-T-C

86909958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 9495405-G-A

86910084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9495279-G-T

86910089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9495274-G-A

86910090-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9495273-T-A

86910090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9495273-T-C

http://identifiers.org/hco/7/GRCh38#86910095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9495268-C-A

86910124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9495239-T-C

86910124-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9495239-T-G

86910134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9495229-A-G

86910323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9495067-T-C

86910355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9495044-G-A

86910635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9494769-A-G

86910639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9494765-T-C

86910789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9494631-T-C

86910870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9494561-T-C

86910971-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9494479-A-T

http://identifiers.org/hco/7/GRCh38#86910994-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9494460-A-C

http://identifiers.org/hco/7/GRCh38#86910995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9494459-C-A

86911329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9493098-T-C

86911656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 9492683-T-C

86911698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 9492641-T-C

http://identifiers.org/hco/7/GRCh38#86911783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9492081-C-A

86911783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9492081-C-T

http://identifiers.org/hco/7/GRCh38#86911821-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9492034-A-C

http://identifiers.org/hco/7/GRCh38#86911879-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9491981-A-C

86911892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 9491964-G-A

86911892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 9491964-G-T

http://identifiers.org/hco/7/GRCh38#86911939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9491917-C-A

86911939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9491917-C-T

http://identifiers.org/hco/7/GRCh38#86911944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9491912-C-A

http://identifiers.org/hco/7/GRCh38#86911967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9491901-C-A

86911967-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9491901-C-G

86911967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9491901-C-T

86912042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9491836-G-A

86912042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9491836-G-T

http://identifiers.org/hco/7/GRCh38#86912053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9491825-C-A

86912053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9491825-C-T

86912076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 9491801-T-C

http://identifiers.org/hco/7/GRCh38#86912235-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9491642-A-C

86912241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 9491636-T-C

http://identifiers.org/hco/7/GRCh38#86912293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9491584-C-A

86912293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9491584-C-T

http://identifiers.org/hco/7/GRCh38#86912296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9491581-C-A

86912324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9491553-A-G

http://identifiers.org/hco/7/GRCh38#86912358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9491520-C-A

http://identifiers.org/hco/7/GRCh38#86912368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9491510-C-A

86912368-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9491510-C-G

86912368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9491510-C-T

http://identifiers.org/hco/7/GRCh38#86912373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9491505-C-A

86912373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9491505-C-T

86912453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9491433-A-G

86912556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9491328-T-C

86912571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9491313-G-A

http://identifiers.org/hco/7/GRCh38#86912579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9491305-C-A

86912854-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9491032-G-C

86912854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9491032-G-T

http://identifiers.org/hco/7/GRCh38#86912886-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9491028-A-C

86912896-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9491018-T-G

86912911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9491010-T-C

86912931-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9490991-A-T

86912966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 9490956-C-T

86913119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 9490803-G-A

86913225-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9490699-T-A

86913225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9490699-T-C

http://identifiers.org/hco/7/GRCh38#86913255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9490669-C-A

86913255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9490669-C-T

86913264-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9490660-T-G

86913442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9490489-T-C

86913786-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9490194-T-A

http://identifiers.org/hco/7/GRCh38#86913884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9490120-C-A

86913918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9490090-A-G

86914119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9489679-T-C

86914257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9489160-G-A

86914261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9489156-T-C

http://identifiers.org/hco/7/GRCh38#86914577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9488850-C-A

86914577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9488850-C-T

86914579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9488848-C-T

http://identifiers.org/hco/7/GRCh38#86914676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#9488783-C-A

86914676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9488783-C-T

86914790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 9487774-T-C

86914793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 9487771-G-A

86914793-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 9487771-G-C

86914867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 9487697-T-C

86914886-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9487683-T-A

86914886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9487683-T-C

http://identifiers.org/hco/7/GRCh38#86914887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9487682-C-A

86914887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9487682-C-T

86914888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9487681-A-G

86914894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9487675-A-G

86914987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9487569-G-A

86914987-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9487569-G-C

86915237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9487421-A-G

http://identifiers.org/hco/7/GRCh38#86915543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9487126-C-A

86915543-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9487126-C-G

86915708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9486986-T-C

86915944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9486811-T-C

86916020-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9486780-T-G

86916101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9486692-G-A

86917581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9486163-A-G

86917603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9486143-C-T

86917631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9486120-T-C

86917634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9486117-A-G

86918172-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9485627-G-C

86918207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9485592-C-T

http://identifiers.org/hco/7/GRCh38#86918413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9485445-C-A

86918533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 9485336-G-T

86918536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 9485333-G-A

86918536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 9485333-G-T

86918605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9485266-A-G

86918650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9485220-C-T

http://identifiers.org/hco/7/GRCh38#86918689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9485185-C-A

86918689-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9485185-C-G

86918710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9485165-A-G

86918853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9485052-T-C

http://identifiers.org/hco/7/GRCh38#86919093-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9484818-C-A

86919093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9484818-C-T

http://identifiers.org/hco/7/GRCh38#86919096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9484815-C-A

86919096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9484815-C-T

86919123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9484799-T-C

86919132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9484788-G-T

86919196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9484728-A-G

86919214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9484715-C-T

http://identifiers.org/hco/7/GRCh38#86919237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9484692-C-A

86919274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 9484655-G-A

http://identifiers.org/hco/7/GRCh38#86919295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9484634-C-A

86919295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 9484634-C-T

86919330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9484600-T-C

http://identifiers.org/hco/7/GRCh38#86919339-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9484591-A-C

86919339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9484591-A-G

86919407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9484527-T-C

86919437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9484497-G-T

86919440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9484494-T-C

86919800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9484167-G-T

86919805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9484162-G-A

86919805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9484162-G-T

86919826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9484148-A-G

86920040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9483950-C-T

86920098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9483899-G-T

86920411-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9483612-T-G

86920489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9483538-A-G

86920604-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9483447-T-A

86920604-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9483447-T-G

86920622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9483428-C-T

86920650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9483401-T-C

http://identifiers.org/hco/7/GRCh38#86920660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9483391-C-A

86920660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9483391-C-T

86923600-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9483159-C-G

86923630-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9483128-T-A

86923630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9483128-T-C

86923680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9483080-A-G

86923699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9483061-T-C

86923791-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9482966-T-A

86923829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9482928-G-A

86923862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9482896-C-T

86923980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9482781-G-A

http://identifiers.org/hco/7/GRCh38#86924099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9482674-C-A

86924127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9482649-C-T

86924322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9482561-G-T

86924423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9482498-T-C

86924479-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9482432-A-T

86924645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9480066-T-C

http://identifiers.org/hco/7/GRCh38#86924665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9480046-C-A

86924914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9479795-T-C

86925061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9479679-A-G

86925065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9479675-T-C

86925087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9479653-A-G

86925184-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9479560-G-C

86925195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9479549-A-G

86925232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9479519-T-C

http://identifiers.org/hco/7/GRCh38#86925402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9478642-C-A

86925402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9478642-C-T

http://identifiers.org/hco/7/GRCh38#86925527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9478532-C-A

86925735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9478329-T-C

86925736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9478328-A-G

86925772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9478296-G-A

86925772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9478296-G-T

86926630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9477972-G-T

86926648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9477950-T-C

86926672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9477925-G-A

86926672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9477925-G-T

86926753-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 9477851-A-T

86926783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 9477821-G-A

http://identifiers.org/hco/7/GRCh38#86926919-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9477685-A-C

86926919-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 9477685-A-T

86926927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9477677-A-G

86926932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9477672-A-G

86926965-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9477619-T-A

86926965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9477619-T-C

http://identifiers.org/hco/7/GRCh38#86926981-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9477603-A-C

86927001-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9477584-T-A

http://identifiers.org/hco/7/GRCh38#86927030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9477556-C-A

86927030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9477556-C-T

86927051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9477539-G-T

86927152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9476917-T-C

86927400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9476442-C-T

86927411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9476430-T-C

86927528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9476289-G-A

86927715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9476120-A-G

http://identifiers.org/hco/7/GRCh38#86927753-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9476091-A-C

86927788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9476061-T-C

http://identifiers.org/hco/7/GRCh38#86927900-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9475951-A-C

86928029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9475826-T-C

86928046-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9475810-T-A

http://identifiers.org/hco/7/GRCh38#86928162-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9475708-A-C

86928260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9475610-A-G

86928709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9474887-T-C

86928717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9474880-G-A

86928746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9474852-T-C

86928746-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9474852-T-G

86928787-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9474815-T-G

86936624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9473952-C-T

86936720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9473859-G-A

86936924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9473650-T-C

86937089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9473487-T-C

86937104-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9473471-G-C

86937415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9473176-A-G

86937520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9473077-G-A

86937550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9473033-T-C

86937726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9472861-G-A

86937815-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9472740-G-C

86937818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9472737-T-C

86937827-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9472728-T-A

86937827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9472728-T-C

http://identifiers.org/hco/7/GRCh38#86938011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9472483-C-A

86938015-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9472479-A-T

86938083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9472429-G-A

86938083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9472429-G-T

86938094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9472418-A-G

http://identifiers.org/hco/7/GRCh38#86938114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9472403-C-A

86938114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9472403-C-T

86938118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 9472399-G-A

86938118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 9472399-G-T

86938136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 9472378-T-C

86938145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 9472369-G-A

86938145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 9472369-G-T

http://identifiers.org/hco/7/GRCh38#86938300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9472206-C-A

86938300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9472206-C-T

86938367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9472133-G-A

86938386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9472114-C-T

86938415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9472080-A-G

86938685-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9471810-A-T

86938775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9471688-G-A

86938775-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9471688-G-C

86938775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9471688-G-T

86938963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 9471500-G-A

86939068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9471399-A-G

http://identifiers.org/hco/7/GRCh38#86939075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9471392-C-A

86939075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9471392-C-T

86939087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9471380-A-G

86939397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 9471284-T-C

86939752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9470975-T-C

86939883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9470838-A-G

86939886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9470835-A-G

86939979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9470751-G-A

86939979-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9470751-G-C

86939979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9470751-G-T

86939990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9470740-A-G

86940072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 9470658-G-A

http://identifiers.org/hco/7/GRCh38#86940142-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9470589-A-C

86940149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9470582-A-G

86940163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9470563-T-C

http://identifiers.org/hco/7/GRCh38#86940178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9470548-C-A

86940196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9470530-T-C

86940592-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9469382-C-G

86940592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9469382-C-T

86940847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9469138-A-G

86940922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9469074-T-C

http://identifiers.org/hco/7/GRCh38#86941201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9468817-C-A

http://identifiers.org/hco/7/GRCh38#86941219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9468796-C-A

86941234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9468781-G-T

http://identifiers.org/hco/7/GRCh38#86941290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9468725-C-A

86941335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9468684-A-G

86941366-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 9468650-C-G

86941457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9468565-A-G

86941577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9468455-G-A

86941577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9468455-G-T

http://identifiers.org/hco/7/GRCh38#86941708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9468316-C-A

86941804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9468245-C-T

86941851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9468198-G-A

86941880-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9468169-A-T

86941955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9468108-A-G

86941955-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9468108-A-T

86941960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9468103-G-A

86941960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9468103-G-T

86942073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 9468014-G-A

86942100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 9467987-T-C

http://identifiers.org/hco/7/GRCh38#86942105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, splice_acceptor_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9467982-C-A

86942110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 9467977-G-A

86942110-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 9467977-G-T

86942117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9467970-C-T

86942137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9467952-G-A

86942137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9467952-G-T

http://identifiers.org/hco/7/GRCh38#86942144-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9467945-A-C

86942144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9467945-A-G

http://identifiers.org/hco/7/GRCh38#86942159-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9467931-A-C

86942159-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9467931-A-T

86942169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9467922-C-T

http://identifiers.org/hco/7/GRCh38#86942171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9467920-C-A

86942171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9467920-C-T

86942193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9467898-G-A

86942193-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9467898-G-C

86942193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9467898-G-T

http://identifiers.org/hco/7/GRCh38#86942201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9467890-C-A

86942268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9467832-A-G

86942302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9467798-T-C

86942440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9467705-C-T

86942825-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9465353-C-G

86943256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9464931-A-G

http://identifiers.org/hco/7/GRCh38#86943262-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9464925-A-C

86943311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9464875-A-G

86943313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9464873-T-C

86943424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9464400-A-G

86943509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9464321-A-G

http://identifiers.org/hco/7/GRCh38#86943924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9463912-C-A

86943924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9463912-C-T

86944039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9463806-C-T

86944549-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9461058-C-G

86944586-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9461023-A-T

86944608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9461001-G-A

86944614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9460995-C-T

86944701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9460912-G-A

86944778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9460841-G-T

86944820-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9460804-T-A

86944820-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9460804-T-G

86944838-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9460795-C-G

86944963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 9460665-T-C

86945132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9460495-T-C

86945132-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9460495-T-G

86945136-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9460490-T-G

http://identifiers.org/hco/7/GRCh38#86945154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9460472-C-A

86945156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9460470-G-T

86945161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9460465-C-T

http://identifiers.org/hco/7/GRCh38#86945176-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9460452-C-A

86945176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9460452-C-T

86945325-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9459937-T-G

http://identifiers.org/hco/7/GRCh38#86945332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9459930-C-A

86945332-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9459930-C-G

86945332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9459930-C-T

86945361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9459898-T-C

86945400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9459834-T-C

86945403-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9459831-A-T

86946815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9459040-C-T

86947058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9451656-G-A

86947210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9451485-T-C

86947440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9451278-T-C

86947453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9451266-G-T

86947456-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9451263-T-G

http://identifiers.org/hco/7/GRCh38#86947576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9451131-C-A

86947576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9451131-C-T

86947585-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9449513-T-A

86947585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9449513-T-C

86947612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9449483-G-T

86947613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9449482-C-T

http://identifiers.org/hco/7/GRCh38#86947636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9449459-C-A

86947636-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9449459-C-G

86947636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9449459-C-T

86947660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9449437-T-C

86947660-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9449437-T-G

86947661-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9449436-G-T

86947685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9449412-C-T

86947781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron_variant, missense_variant
orthologous variants: 9449320-G-A

86947781-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron_variant, missense_variant
orthologous variants: 9449320-G-C

http://identifiers.org/hco/7/GRCh38#86947807-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9449294-C-A

http://identifiers.org/hco/7/GRCh38#86948013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#9449085-C-A

86948013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron_variant, undefined
orthologous variants: 9449085-C-T

86948021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron_variant, undefined
orthologous variants: 9449077-G-A

86948021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron_variant, undefined
orthologous variants: 9449077-G-T

86948049-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron_variant, undefined
orthologous variants: 9449048-T-A

http://identifiers.org/hco/7/GRCh38#86948067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#9449028-C-A

86948276-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron_variant, undefined
orthologous variants: 9448860-C-G

86948342-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9448796-G-C

86948394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9448772-C-T

86948507-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9448663-G-C

86948625-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9448552-T-A

86948995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9448236-T-C

86953331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9446118-A-G

86953558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9445913-G-A

86953615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9445842-A-G

86953680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9445799-C-T

86953700-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9445779-T-G

86953867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9445178-C-T

86953906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9445142-G-A

86954414-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9444638-G-C

86954437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9444615-A-G

86954542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9444510-T-C

86954844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9444161-T-C

86954844-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9444161-T-G

86955004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9444009-A-G

86955145-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9443869-T-G

86955275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9443744-G-A

86955302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9443716-G-T

86955390-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9443633-T-A

http://identifiers.org/hco/7/GRCh38#86955792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9443287-C-A

86955828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9443249-A-G

86955834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9443243-T-C

86955834-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9443243-T-G

86955864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9443210-C-T

86956173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9442992-T-C

86956461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9442729-T-C

86956571-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9442671-G-C

86956866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9442332-A-G

86957052-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9442157-T-G

86957193-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9442001-A-T

86957353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9441870-T-C

86957399-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9441827-A-T

86957500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9441687-A-G

86957515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9441672-C-T

86957595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9441607-A-G

86957947-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9441467-C-G

http://identifiers.org/hco/7/GRCh38#86958101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9441325-C-A

86958358-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9440394-T-A

86958358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9440394-T-C

86958600-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9440173-A-T

86958730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9440050-G-A

86958749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9440027-C-T

86960614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9436692-A-G

86960614-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9436692-A-T

86960616-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9436690-T-G

86960656-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9436654-G-C

86960774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9436546-G-T

86960877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9436417-G-A

86961242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9436023-T-C

86961329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9435988-T-C

86961329-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9435988-T-G

86961337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9435980-G-A

86961538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9435754-A-G

86961770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9435397-G-A

86961774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9435331-T-C

86961820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9435282-T-C

http://identifiers.org/hco/7/GRCh38#86961852-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9435252-A-C

86961914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9435197-T-C

86961959-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9435157-C-G

86962293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9433920-A-G

http://identifiers.org/hco/7/GRCh38#86962309-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9433904-A-C

86962517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9433723-G-A

86962561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9433699-G-A

86962602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9433659-T-C

86963013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9433101-G-A

86963192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9432914-G-A

86963523-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9432602-C-G

86963725-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9432421-T-A

86963934-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9432231-A-T

86964088-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9432088-T-A

86964123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9432059-C-T

http://identifiers.org/hco/7/GRCh38#86964408-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9431809-A-C

86964579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9430926-G-T

86964681-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9430832-A-T

86964723-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9430795-T-A

86964753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9430765-A-G

86964753-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9430765-A-T

86964839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9430465-T-C

http://identifiers.org/hco/7/GRCh38#86965152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9430147-C-A

86965152-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9430147-C-G

86965152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9430147-C-T

86965171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9430129-T-C

86965200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9430100-C-T

86965535-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9429822-C-G

86965730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9429523-A-G

86965795-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9429439-T-G

86965887-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 9429301-G-C

86965901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 9429287-G-A

86965901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 9429287-G-T

http://identifiers.org/hco/7/GRCh38#86965903-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9429285-A-C

86965944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 9429245-G-A

86965944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 9429245-G-T

86965954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 9429234-T-C

86965954-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 9429234-T-G

86965983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9429211-T-C

86966046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9429147-A-G

86966721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9428255-G-A

86968177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9424430-A-G

http://identifiers.org/hco/7/GRCh38#86968288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9424106-C-A

86968473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9423878-A-G

http://identifiers.org/hco/7/GRCh38#86968519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9423834-C-A

86968519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9423834-C-T

86968521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9423832-T-C

86968642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9423717-G-A

http://identifiers.org/hco/7/GRCh38#86968686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9423686-C-A

86968771-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9423605-A-T

86968840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9423557-T-C

86968901-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9423495-T-G

86969283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9423149-T-C

86969468-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9422074-T-A

86969468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9422074-T-C

86969642-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9421893-T-A

86969642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9421893-T-C

86969698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9421830-C-T

86969710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9421818-C-T

http://identifiers.org/hco/7/GRCh38#86970261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9420532-C-A

86970261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9420532-C-T

86970434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9420356-G-A

86970861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9419960-A-G

86970886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9419935-T-C

86971127-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9419685-T-G

86971152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9419664-C-T

86971279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9419541-C-T

86971757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9418871-T-C

http://identifiers.org/hco/7/GRCh38#86972658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9418588-C-A

http://identifiers.org/hco/7/GRCh38#86972833-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9418420-A-C

86972899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9418354-T-C

86973149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9418143-T-C

86973155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9418137-G-A

86973155-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9418137-G-C

86973341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9417955-T-C

http://identifiers.org/hco/7/GRCh38#86973448-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9417870-A-C

86973495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9417834-A-G

86973502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9417827-A-G

86973605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9417616-A-G

86973764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9416101-A-G

86973911-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9415954-A-T

86974026-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9415865-T-G

86974038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9415853-A-G

86974052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9415831-T-C

86974081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9415803-C-T

86974084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9415800-T-C

86974372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9415542-T-C

86974540-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9415379-G-C

86974599-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9415217-G-C

http://identifiers.org/hco/7/GRCh38#86975369-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9414190-A-C

http://identifiers.org/hco/7/GRCh38#86975393-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9414166-A-C

86975553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9414002-T-C

86975580-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9413975-T-A

86975580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9413975-T-C

86975665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9413861-C-T

86976013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9413562-T-C

86976071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9413514-T-C

86976155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9413429-C-T

http://identifiers.org/hco/7/GRCh38#86976186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9413398-C-A

86976259-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9413331-C-G

86976259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9413331-C-T

86976351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9413237-G-A

86976351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9413237-G-T

86976404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9413181-G-A

86976498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9412638-C-T

86976672-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9412488-G-C

86976830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9412324-A-G

86976931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9412221-C-T

86977029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9412118-A-G

86977127-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9412029-C-G

86977402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9411739-G-A

86977411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9411565-T-C

86977858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9411164-A-G

86988813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9403444-C-T

http://identifiers.org/hco/7/GRCh38#86988834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9403423-C-A

86989879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9402114-T-C

86990635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9401342-G-A

86990643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9401334-G-T

86993290-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9400455-T-A

86993312-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9400441-A-T

86993485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9400288-T-C

86993698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9400107-C-T

86993763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9400045-A-G

86994217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9398138-C-T

86994284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9398074-G-T

86994792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9397568-A-G

86994823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9397526-G-A

86994823-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9397526-G-C

86995190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9397179-C-T

86998139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9396926-G-A

86999019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9396179-T-C

http://identifiers.org/hco/7/GRCh38#86999020-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9396178-A-C

86999023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9396175-G-A

86999032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9396166-A-G

86999182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9396026-G-A

86999187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9396024-T-C

http://identifiers.org/hco/7/GRCh38#86999213-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9395998-A-C

86999453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9395733-T-C

86999643-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9395526-A-T

87000077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9395229-T-C

87000077-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9395229-T-G

87000166-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9395144-T-A

87000313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9394955-C-T

87000536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9394715-G-A

87000739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9394509-A-G

87000912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9394345-C-T

87001197-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9393766-A-T

87001722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9393232-G-A

87001797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9393166-T-C

87001901-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9393066-G-C

87002014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9392954-A-G

http://identifiers.org/hco/7/GRCh38#87002450-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9392646-A-C

http://identifiers.org/hco/7/GRCh38#87002704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9392418-C-A

87002710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9392412-G-A

87002910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9392263-A-G

87003021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9392165-T-C

87003223-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9391675-G-C

87003997-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9390046-C-G

87004031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9390009-A-G

87004457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9389580-A-G

87004677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9389367-C-T

87004698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9389347-G-A

http://identifiers.org/hco/7/GRCh38#87004700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9389345-C-A

87004700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9389345-C-T

87004938-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9389110-T-G

87005010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9389039-G-A

http://identifiers.org/hco/7/GRCh38#87005423-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9387960-A-C

87005427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9387956-C-T

87009296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9375516-A-G

87009623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9375224-C-T

87009812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9375089-G-T

87009844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9375060-G-A

87010347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9374404-G-A

87011495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9368402-G-A

87012525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9367759-T-C

87012669-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9367700-G-C

87012701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9367676-T-C

87012889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9367487-T-C

87013507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9367215-G-A

87013996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9367023-T-C

http://identifiers.org/hco/7/GRCh38#87014185-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9366842-A-C

87014193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9366841-T-C

87014527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9366541-G-T

87014580-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9366478-G-C

87014739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9366320-G-A

87014739-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9366320-G-C

87014837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9366213-T-C

87014841-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9366209-A-T

87015012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9366033-G-A

87015147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9365906-T-C

http://identifiers.org/hco/7/GRCh38#87015239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9365615-C-A

http://identifiers.org/hco/7/GRCh38#87015291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9365566-C-A

87015291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9365566-C-T

87015993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9364543-T-C

87016198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9364341-T-C

87016217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9364322-G-A

http://identifiers.org/hco/7/GRCh38#87017044-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9363101-A-C

87017044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9363101-A-G

87017049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9363097-T-C

87017339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9362818-C-T

87017359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9362801-A-G

87017413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9362746-T-C

87018463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9362222-G-A

87018725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9361982-T-C

87019561-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9361481-C-G

http://identifiers.org/hco/7/GRCh38#87019606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9361434-C-A

87019765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9361274-T-C

87019816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9361223-G-A

87019822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9361217-T-C

87020305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9353508-A-G

87020443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9353395-T-C

87020521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9353322-G-A

87020596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9353249-G-A

87020724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9353108-C-T

http://identifiers.org/hco/7/GRCh38#87021035-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9352805-A-C

87021035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9352805-A-G

87021068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9352769-C-T

87021174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9352680-C-T

87021294-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9352570-C-G

87021497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9352351-T-C

http://identifiers.org/hco/7/GRCh38#87021546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9352304-C-A

87021619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9352242-T-C

87025397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9351594-T-C

87025434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9351566-A-G

87025605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9351421-C-T

87026209-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9350941-T-A

87026295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9350883-G-A

87026295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9350883-G-T

87026317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9350863-T-C

87026335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9350844-A-G

87026376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9350803-T-C

87026376-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9350803-T-G

http://identifiers.org/hco/7/GRCh38#87026518-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9350670-A-C

87026519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9350669-A-G

87026596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9350590-T-C

87026628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9350558-G-A

http://identifiers.org/hco/7/GRCh38#87026951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9350055-C-A

87026959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9350047-T-C

87027131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9349477-T-C

87027292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9349073-G-A

87027353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9349022-A-G

87027377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9348731-A-G

87027448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9348660-T-C

87027668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9348472-A-G

87027733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron_variant, undefined
orthologous variants: 9348411-T-C

87027827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9348341-T-C

87027842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9348326-G-A

87027903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9348273-A-G

87028069-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9347919-T-A

87028169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9347817-G-A

http://identifiers.org/hco/7/GRCh38#87029351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9345525-C-A

87029371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9345505-G-T

87029572-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9345291-T-A

87031302-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9344858-C-G

87031425-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9344745-C-G

87031685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9343852-G-T

87031696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9343841-A-G

87031842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9343696-C-T

87032254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9338991-T-C

87032260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9338985-T-C

87032747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9338566-T-C

87032969-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9338351-T-A

87033089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9338261-G-A

http://identifiers.org/hco/7/GRCh38#87033124-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9338229-A-C

87033180-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9338175-A-T

87033332-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9338011-A-T

http://identifiers.org/hco/7/GRCh38#87033333-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9338010-A-C

87033333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9338010-A-G

87033333-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9338010-A-T

http://identifiers.org/hco/7/GRCh38#87033436-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9337917-A-C

87033653-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9337729-T-A

http://identifiers.org/hco/7/GRCh38#87033912-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9337323-A-C

87037544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9333912-G-A

87037599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9333855-T-C

87037661-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9333792-T-A

87037776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9333675-T-C

87038054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9333440-A-G

87038064-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9333430-T-A

87038107-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9333378-T-A

87038166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9333171-C-T

http://identifiers.org/hco/7/GRCh38#87038429-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9332903-A-C

87038491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9332844-G-A

87051134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9324633-C-T

87051190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9324578-G-A

http://identifiers.org/hco/7/GRCh38#87051204-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9324564-A-C

87051251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9324513-T-C

http://identifiers.org/hco/7/GRCh38#87051267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9324497-C-A

87051277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9324491-T-C

87051334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9324443-A-G

87051446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9324360-T-C

87051492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9324313-T-C

87051643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9324203-T-C

87051737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9324135-C-T

87051744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9324129-C-T

87051777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9324096-C-T

87052031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9323835-G-A

http://identifiers.org/hco/7/GRCh38#87052134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9323732-C-A

87053766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9322810-A-G

87053802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9322774-C-T

http://identifiers.org/hco/7/GRCh38#87054731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9321120-C-A

87054731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9321120-C-T

87054732-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9321119-A-T

87055329-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9320573-T-A

87055352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9320555-T-C

87055720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9320198-A-G

87055816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9320102-C-T

87055826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9320093-G-A

87055838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9320073-T-C

87055986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9319932-A-G

87056294-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9319628-G-C

87056410-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9319524-G-C

http://identifiers.org/hco/7/GRCh38#87057136-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9318784-A-C

87057209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9318718-C-T

87057394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9318532-G-A

87057516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9318420-T-C

87057569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9318366-G-A

87057650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9318284-A-G

87057740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9317966-T-C

87057741-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9317965-T-A

87058403-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9317315-A-T

87058585-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9317129-G-C

87058755-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9316963-T-A

87058755-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9316963-T-G

87058911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9316841-G-A

87059216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: intron variant
orthologous variants: 9316553-A-G

87059368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, synonymous_variant
orthologous variants: 9316414-T-C

http://identifiers.org/hco/7/GRCh38#87059392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9316390-C-A

87059392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, synonymous_variant
orthologous variants: 9316390-C-T

http://identifiers.org/hco/7/GRCh38#87059440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9316342-C-A

87059440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, synonymous_variant
orthologous variants: 9316342-C-T

87059452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, synonymous_variant
orthologous variants: 9316330-G-A

87059452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, synonymous_variant
orthologous variants: 9316330-G-T

87059473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 5_prime_UTR_variant, intron_variant, stop_gained, synonymous_variant
orthologous variants: 9316309-C-T

87059474-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 9316308-A-T

http://identifiers.org/hco/7/GRCh38#87059520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9316267-C-A

87059520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 5 prime UTR variant
orthologous variants: 9316267-C-T

87059538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 5 prime UTR variant
orthologous variants: 9316253-C-T

87059544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 9316247-G-A

87059544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 9316247-G-T

http://identifiers.org/hco/7/GRCh38#87059598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#9316224-C-A

87059598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21945
most severe consequence: 5 prime UTR variant
orthologous variants: 9316224-C-T