123973271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 124939816-G-A

123973271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 124939816-G-T

http://identifiers.org/hco/12/GRCh38#123973322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#124939887-C-A

123973322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 124939887-C-T

http://identifiers.org/hco/12/GRCh38#123973741-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124940253-C-A

123973741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124940253-C-T

123973822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124940331-A-G

123973822-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124940331-A-T

123973840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124940352-G-A

123974031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124940580-T-C

123974032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124940581-G-A

123974032-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124940581-G-T

123974072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124940617-G-A

123974072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124940617-G-T

123974192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124940667-T-C

123974197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124940672-T-C

123974217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 124940692-C-T

123974251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124940727-T-C

123974251-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124940727-T-G

http://identifiers.org/hco/12/GRCh38#123974260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124940736-C-A

123974476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124940919-G-T

123974961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124941393-G-A

123974975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124941407-A-G

123974976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124941408-G-A

123975005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124941431-G-A

123975143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124941535-A-G

123975177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124941566-G-A

123976106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124941873-T-C

123976391-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124942133-T-G

http://identifiers.org/hco/12/GRCh38#123976469-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124942205-A-C

123976469-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124942205-A-T

123976528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124942235-A-G

123980140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124943036-T-C

123980223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124943113-G-A

123980293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124943175-G-T

123980525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124943380-T-C

123980595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124943430-G-A

123980661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124943494-C-T

123980689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124943517-A-G

http://identifiers.org/hco/12/GRCh38#123980781-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124943598-A-C

123981750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124944291-C-T

123981957-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124944473-T-A

123982789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124945296-G-A

123982789-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124945296-G-T

http://identifiers.org/hco/12/GRCh38#123983486-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124945815-A-C

123983486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124945815-A-G

123983945-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124946208-C-G

http://identifiers.org/hco/12/GRCh38#123984398-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124946519-A-C

123984576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124946629-A-G

123986016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124948032-A-G

123986383-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124948300-T-G

http://identifiers.org/hco/12/GRCh38#123986866-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124948652-A-C

123986866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124948652-A-G

123986869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124948655-G-T

123986991-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124948728-C-G

123986992-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124948729-C-G

123987061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124948785-G-A

http://identifiers.org/hco/12/GRCh38#123987874-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124949467-C-A

123987995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124949561-A-G

123988105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124949668-G-A

123988105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124949668-G-T

123988109-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124949672-T-A

123988129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124949688-T-C

123988151-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124949710-C-G

123988151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124949710-C-T

123991029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124950922-G-A

123991216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124951094-A-G

http://identifiers.org/hco/12/GRCh38#123991340-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124951168-A-C

123991636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124951423-G-A

123991654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124951439-A-G

123991785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124951568-C-T

123992030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124951775-A-G

http://identifiers.org/hco/12/GRCh38#123993817-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124952994-A-C

123993875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124953027-C-T

123993906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124953049-A-G

123994028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124953123-C-T

123994150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124953180-G-A

123996341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124954116-G-A

123996498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124954271-G-A

123996498-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124954271-G-C

123996626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124954387-G-A

123996673-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124954407-T-G

123996687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124954421-T-C

123996808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124954500-C-T

123996855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124954528-A-G

123997028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124954635-A-G

123997391-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124954951-C-G

123997391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124954951-C-T

http://identifiers.org/hco/12/GRCh38#123997588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124955076-C-A

123997611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124955093-T-C

http://identifiers.org/hco/12/GRCh38#123997719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124955198-C-A

123997738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124955214-G-A

123997847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 124955284-T-C

123997967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124955398-T-C

123998017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124955448-G-A

124010508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124961070-G-T

124010678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124961222-C-T

124010729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124961273-A-G

124010909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124961437-T-C

124011365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124961757-A-G

http://identifiers.org/hco/12/GRCh38#124011383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124961774-C-A

124011397-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124961788-G-T

http://identifiers.org/hco/12/GRCh38#124011554-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124962024-A-C

124011554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124962024-A-G

124011554-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124962024-A-T

http://identifiers.org/hco/12/GRCh38#124011580-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124962047-A-C

124011580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124962047-A-G

124011580-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124962047-A-T

http://identifiers.org/hco/12/GRCh38#124011596-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124962063-A-C

124011596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124962063-A-G

124011596-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124962063-A-T

124011860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124962319-G-A

124011905-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124962367-G-C

124011905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124962367-G-T

124012004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124962466-G-A

124012095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124962555-G-A

http://identifiers.org/hco/12/GRCh38#124012097-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124962557-A-C

124012097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124962557-A-G

124012246-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 124962709-C-G

124012246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 124962709-C-T

124012312-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 124962775-G-C

124012675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 124963138-G-A

http://identifiers.org/hco/12/GRCh38#124013218-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124963654-A-C

124013218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124963654-A-G

http://identifiers.org/hco/12/GRCh38#124013243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124963677-C-A

124013243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124963677-C-T

http://identifiers.org/hco/12/GRCh38#124013256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124963690-C-A

124013256-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124963690-C-G

124013256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124963690-C-T

http://identifiers.org/hco/12/GRCh38#124013356-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124963770-A-C

124013356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124963770-A-G

124013507-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124963917-T-A

124013575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124963985-T-C

124013575-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124963985-T-G

124013827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124964250-G-T

124013995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124964392-A-G

http://identifiers.org/hco/12/GRCh38#124014001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124964398-C-A

124014216-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124964570-G-C

124014216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124964570-G-T

http://identifiers.org/hco/12/GRCh38#124014849-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124965135-A-C

124014867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124965149-T-C

124015106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124965374-T-C

124015118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124965386-T-C

http://identifiers.org/hco/12/GRCh38#124015169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124965437-C-A

124015169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124965437-C-T

124015176-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124965444-T-A

124015214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124965482-G-T

124015228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124965496-G-A

124015333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124965601-G-T

124015373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124965640-T-C

124015381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124965648-C-T

124029582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124969784-G-A

124030922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124972164-C-T

124031141-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124972381-G-C

124032124-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124972594-G-T

124032297-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124972766-C-G

124032309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124972773-A-G

124032328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124972791-G-A

124032328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124972791-G-T

124032369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124972831-C-T

124033599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124973232-A-G

124033655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124973266-G-T

124037222-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124977499-G-C

124037483-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124977649-T-G

124038506-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124978522-T-G

124038597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124978614-G-A

124038741-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124978717-T-G

124039156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124979049-A-G

124042895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124983091-C-T

124042896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124983092-G-A

124043497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124983785-A-G

124043752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124984021-T-C

124043773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124984041-A-G

124043847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124984100-G-A

124043935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124984211-C-T

124044006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124984270-C-T

124044088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124984343-G-A

124044089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124984344-T-C

http://identifiers.org/hco/12/GRCh38#124071229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124988834-C-A

124071229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124988834-C-T

124071278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124988878-T-C

124071293-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124988893-T-G

124071342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124988954-A-G

124071513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124989131-G-T

124071532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124989150-C-T

124087883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124990404-G-A

124087883-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124990404-G-C

124087883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124990404-G-T

124087930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124990450-T-C

124088005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124990514-G-T

124088018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124990526-A-G

124088041-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124990549-T-A

124088062-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124990570-A-T

124088175-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124990661-T-G

124088284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124990752-G-T

http://identifiers.org/hco/12/GRCh38#124088338-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124990782-C-A

http://identifiers.org/hco/12/GRCh38#124088476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124990913-C-A

124088476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124990913-C-T

124090628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124993694-G-T

124090629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124993695-G-A

124090929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124993961-C-T

124111306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125000491-A-G

124111378-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125000532-T-G

124111452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125000605-C-T

124111473-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125000626-A-T

124111642-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125000778-G-C

124111643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125000779-G-A

124114458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125001894-C-T

124114710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125002107-G-A

124114735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125002123-G-A

124116089-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125004946-C-G

124116090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125004947-A-G

124116099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125004955-A-G

124116099-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125004955-A-T

124116232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125005062-G-A

124116278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125005103-C-T

124116288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125005113-G-A

124120643-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125008138-T-A

124120643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125008138-T-C

124120659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125008154-G-A

124120821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125008288-T-C

124123464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125011637-G-T

124123758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125011941-A-G

124123814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125011990-G-A

124123872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125012041-G-A

124125499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125013457-T-C

124125500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125013458-G-T

124170862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125027759-C-T

124171460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125028247-A-G

124171668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125028311-G-A

124171673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125028316-T-C

http://identifiers.org/hco/12/GRCh38#124171736-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125028380-A-C

124171761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125028405-G-A

124171764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125028408-G-A

124171873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125028518-G-A

124175067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125030436-G-T

124185203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125034878-T-C

124185292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125034962-C-T

124188680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 125037536-A-G

124191693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125041171-G-A

124191795-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125041267-T-A

124191915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125041378-G-A

124192055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125041496-T-C

124193103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125042659-G-A

124193148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125042728-C-T

124193157-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125042737-T-G

124193180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125042760-G-A

124193329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125042897-G-A

124194743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125043725-C-T

124194744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125043726-G-A

124194766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125043762-A-G

124194998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125043978-A-G

124195259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125044168-G-A

124195481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125044339-C-T

124217840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125048157-G-A

124217863-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125048174-C-G

124217972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125048271-G-A

124218041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125048338-A-G

124218133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125048429-A-G

124218202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125048505-A-G

124218251-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125048559-G-C

124224440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125049491-G-T

124224444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125049495-G-A

124224456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125049507-A-G

http://identifiers.org/hco/12/GRCh38#124224479-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125049529-A-C

http://identifiers.org/hco/12/GRCh38#124224592-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125049626-A-C

124224592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125049626-A-G

124224608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125049642-G-A

124224808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125049793-G-A

124224808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125049793-G-T

124224947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125049922-C-T

124225046-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125049989-T-G

124225392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125050250-A-G

124225488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125050344-A-G

124229071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125051640-G-A

124229407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125052053-C-T

124229496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125052151-C-T

124229774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125052404-A-G

124229774-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125052404-A-T

124229845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125052475-C-T

124239062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron variant
orthologous variants: 125057138-C-T

124239128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron variant
orthologous variants: 125057220-T-C

124239128-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron variant
orthologous variants: 125057220-T-G

124239370-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron variant
orthologous variants: 125057441-A-T

124243685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron variant
orthologous variants: 125060001-C-T

124249102-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron variant
orthologous variants: 125062033-C-G

124249175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron variant
orthologous variants: 125062105-C-T

124249206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron variant
orthologous variants: 125062120-A-G

124249287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron variant
orthologous variants: 125062200-C-T

124249500-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron variant
orthologous variants: 125062354-A-T

124249572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron variant
orthologous variants: 125062402-G-A

124249593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron variant
orthologous variants: 125062408-G-A

124249593-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron variant
orthologous variants: 125062408-G-C

http://identifiers.org/hco/12/GRCh38#124249684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125062502-C-A

124278249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron variant
orthologous variants: 125064831-A-G

124278314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron variant
orthologous variants: 125064883-A-G

124278388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron variant
orthologous variants: 125064955-C-T

124278421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron variant
orthologous variants: 125064977-C-T

124278686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, undefined
orthologous variants: 125065241-C-T

124278786-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron variant
orthologous variants: 125065327-C-G

124278795-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron variant
orthologous variants: 125065336-C-G

124282773-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron variant
orthologous variants: 125069845-G-C

124283745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron variant
orthologous variants: 125070911-G-A

124283745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron variant
orthologous variants: 125070911-G-T

124289857-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron variant
orthologous variants: 125075479-C-G

124289920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron variant
orthologous variants: 125075525-G-A

124290076-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron variant
orthologous variants: 125075640-C-G

124290248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron variant
orthologous variants: 125075711-G-A

124290248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron variant
orthologous variants: 125075711-G-T

124290333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron variant
orthologous variants: 125075796-T-C

124291744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron variant
orthologous variants: 125077555-C-T

http://identifiers.org/hco/12/GRCh38#124291976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125077713-C-A

124291976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron variant
orthologous variants: 125077713-C-T

http://identifiers.org/hco/12/GRCh38#124292555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125078102-C-A

124292555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron variant
orthologous variants: 125078102-C-T

124292716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron variant
orthologous variants: 125078285-C-T

124292818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron variant
orthologous variants: 125078383-G-A

124292861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron variant
orthologous variants: 125078413-T-C

http://identifiers.org/hco/12/GRCh38#124295173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125080426-C-A

124295173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 125080426-C-T

124295192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 125080451-G-A

124295192-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 125080451-G-C

124295192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 125080451-G-T

http://identifiers.org/hco/12/GRCh38#124295208-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125080467-A-C

124295208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 125080467-A-G

124295208-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 125080467-A-T

http://identifiers.org/hco/12/GRCh38#124295390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125080595-C-A

124295390-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 125080595-C-G

124295390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 125080595-C-T

http://identifiers.org/hco/12/GRCh38#124295420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#125080622-C-A

124295420-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 125080622-C-G

124295420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 125080622-C-T

124296807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron variant
orthologous variants: 125081391-T-C

124296832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron variant
orthologous variants: 125081416-G-A

124296926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron_variant, undefined
orthologous variants: 125081493-C-T

124297159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron variant
orthologous variants: 125081664-C-T

124297182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron variant
orthologous variants: 125081685-A-G

124297246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron variant
orthologous variants: 125081749-C-T

124297428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron variant
orthologous variants: 125081894-A-G

124297445-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron variant
orthologous variants: 125081912-C-G

124297445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron variant
orthologous variants: 125081912-C-T

124297730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron variant
orthologous variants: 125082153-C-T

124297799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron variant
orthologous variants: 125082211-G-A

http://identifiers.org/hco/12/GRCh38#124303655-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125085792-A-C

124303655-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron variant
orthologous variants: 125085792-A-T

124303701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron variant
orthologous variants: 125085812-C-T

124311981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron variant
orthologous variants: 125087611-G-A

124311981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron variant
orthologous variants: 125087611-G-T

124311990-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron variant
orthologous variants: 125087627-T-A

124311990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron variant
orthologous variants: 125087627-T-C

124311990-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron variant
orthologous variants: 125087627-T-G

http://identifiers.org/hco/12/GRCh38#124314141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#125088300-C-A

124314141-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron variant
orthologous variants: 125088300-C-G

124314141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron variant
orthologous variants: 125088300-C-T

124314179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: intron variant
orthologous variants: 125088323-C-T

124314360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: synonymous variant
orthologous variants: 125088504-G-A

124314484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27051
most severe consequence: stop gained
orthologous variants: 125088628-C-T