45361630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 122425494-C-T

45361746-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 122425626-A-T

45361893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 122425776-A-G

45361915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 122425798-G-A

45361930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 122425813-G-A

45361930-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 122425813-G-C

45361930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 122425813-G-T

45362130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 122425999-G-A

45362246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122426116-A-G

45362307-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122426199-C-G

45362309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122426201-T-C

45362434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122426334-G-A

45362439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122426339-G-A

45362694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122426475-T-C

45362800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122426578-G-A

45363107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122426963-T-C

45363313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122427305-T-C

45363462-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122427450-T-G

http://identifiers.org/hco/15/GRCh38#45363486-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122427474-A-C

http://identifiers.org/hco/15/GRCh38#45363515-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122427503-A-C

45363530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122427518-G-A

45363530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122427518-G-T

45363554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122427546-A-G

45363676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122427654-T-C

45363688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122427665-G-A

45363688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122427665-G-T

45363703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122427680-G-T

45363766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122427722-T-C

45363828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122427784-G-A

45363828-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122427784-G-T

http://identifiers.org/hco/15/GRCh38#45363829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122427785-C-A

45363871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122427824-T-C

45363871-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122427824-T-G

http://identifiers.org/hco/15/GRCh38#45363877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122427830-C-A

45363877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122427830-C-T

45363886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 122427839-T-C

45364101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122428060-C-T

45364197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122428373-T-C

http://identifiers.org/hco/15/GRCh38#45364583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122428445-C-A

45364583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122428445-C-T

45364686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122428532-G-A

45364686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122428532-G-T

45364874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122428695-A-G

45364875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122428696-A-G

45364929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122428732-T-C

45364938-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122428741-T-A

45365402-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122430260-T-G

http://identifiers.org/hco/15/GRCh38#45365441-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122430295-A-C

45365441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122430295-A-G

45365443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122430297-A-G

http://identifiers.org/hco/15/GRCh38#45365515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122430362-C-A

45365515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122430362-C-T

45365910-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122430739-G-C

45365910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122430739-G-T

45366055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 122430869-T-C

45366193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 122431007-G-A

45366240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122431058-T-C

45366339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122431142-A-G

45366467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 122431269-A-G

45366661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122431472-C-T

45367738-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122432687-C-G

45367972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122432889-A-G

http://identifiers.org/hco/15/GRCh38#45367975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122432892-C-A

45367975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122432892-C-T

45368014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122432930-C-T

45368160-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 122433076-C-G

45368160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 122433076-C-T

http://identifiers.org/hco/15/GRCh38#45368279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122433195-C-A

45368279-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122433195-C-G

http://identifiers.org/hco/15/GRCh38#45368444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122433230-C-A

45368680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122433281-C-T

45368784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122433387-G-A

45368897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122433478-C-T

45368926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122433507-G-A

45369024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122433805-C-T

45369253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122433989-G-T

45369579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122434316-G-A

45369611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122434348-G-A

45369611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122434348-G-T

http://identifiers.org/hco/15/GRCh38#45369650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122434380-C-A

45369650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122434380-C-T

45369659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122434389-A-G

http://identifiers.org/hco/15/GRCh38#45369689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122434422-C-A

45369689-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122434422-C-G

45369689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122434422-C-T

45369737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122434682-A-G

45369769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122434713-G-T

http://identifiers.org/hco/15/GRCh38#45369772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122434716-C-A

45369788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122434731-G-A

http://identifiers.org/hco/15/GRCh38#45369813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122434757-C-A

45369813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122434757-C-T

45369831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122434763-T-C

45371907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122435855-G-T

45371967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122435914-G-A

45372030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122435950-G-A

45372129-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122436029-G-C

45372273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122436174-T-C

45375580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122439185-T-C

45375664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122439310-G-A

45375682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122439328-A-G

45375917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122439524-A-G

45375936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122439543-T-C

45375938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122439545-G-A

45376011-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122439618-C-G

45376011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122439618-C-T

45376063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122439682-T-C

45376092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122439711-C-T

45376223-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122439837-T-G

45376244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122439863-A-G

45376444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122439983-G-A

45376539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122440083-A-G

45376541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122440085-G-A

45376541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122440085-G-T

45376569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122440119-C-T

http://identifiers.org/hco/15/GRCh38#45376590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122440139-C-A

45376590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 122440139-C-T

45376595-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 122440144-C-G

45376749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 122440298-C-T

45376891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122440415-A-G

45376923-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122440446-T-A

45376923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122440446-T-C

http://identifiers.org/hco/15/GRCh38#45377001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122440506-C-A

http://identifiers.org/hco/15/GRCh38#45377204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122440700-C-A

45377204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122440700-C-T

45377243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122440737-A-G

http://identifiers.org/hco/15/GRCh38#45377268-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122440762-C-A

45377268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122440762-C-T

45377416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122440872-T-C

45377481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122440915-T-C

45377630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122441217-G-A

http://identifiers.org/hco/15/GRCh38#45377638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122441225-C-A

45377638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122441225-C-T

45377748-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122441333-T-A

45377748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122441333-T-C

45377748-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122441333-T-G

45377764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122441366-C-T

http://identifiers.org/hco/15/GRCh38#45377791-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122441394-A-C

http://identifiers.org/hco/15/GRCh38#45377824-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122441426-C-A

45377909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122441474-T-C

http://identifiers.org/hco/15/GRCh38#45377977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122441529-C-A

45377977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122441529-C-T

http://identifiers.org/hco/15/GRCh38#45377983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122441535-C-A

45378288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122441616-G-A

45378288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122441616-G-T

45378290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122441618-T-C

http://identifiers.org/hco/15/GRCh38#45378385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#122441629-C-A

45378385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant, undefined
orthologous variants: 122441629-C-T

http://identifiers.org/hco/15/GRCh38#45378448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122441692-C-A

45378448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 122441692-C-T

45378465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 122441709-G-A

45378465-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 122441709-G-C

45378465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 122441709-G-T

45378509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122441754-G-A

45378509-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122441754-G-C

45378509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122441754-G-T

45378694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122441851-G-A

45378694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122441851-G-T

http://identifiers.org/hco/15/GRCh38#45378699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122441855-C-A

45378699-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122441855-C-G

45378699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122441855-C-T

45379302-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122442305-T-G

45380284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122442607-G-A

http://identifiers.org/hco/15/GRCh38#45380308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122442627-C-A

45380391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122442711-A-G

45380499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 122442819-G-T

45380506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122442826-C-T

45380686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122443209-G-A

45380726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122443243-G-A

45380734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122443251-G-A

45380745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122443262-T-C

45381812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122443466-A-G

45381936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122444543-G-T

45382056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122444650-C-T

45382990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122445394-A-G

45383080-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122445520-A-T

45385312-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122446168-A-T

45385564-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122446617-G-C

45386531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122446889-T-C

45386609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122446972-T-C

45386646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122447006-C-T

45387284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122447741-T-C

45390587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122449139-T-C

45390829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122449327-T-C

45390829-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122449327-T-G

45390965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122449425-A-G

45390974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122449432-T-C

45391017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122449471-A-G

45391098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122449552-T-C

45391557-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122449698-T-A

45391593-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122449723-G-C

45391631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122449749-C-T

45391932-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122449987-T-G

45392282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 122450190-G-A

45392662-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122450827-C-G

http://identifiers.org/hco/15/GRCh38#45392760-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122450883-A-C

45392760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122450883-A-G

45393078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122455718-T-C

45393502-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122456075-G-C

45394493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122456305-G-A

45394547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122456361-G-A

45394547-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122456361-G-C

http://identifiers.org/hco/15/GRCh38#45394552-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122456369-A-C

45394889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122456724-C-T

45395165-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122456994-C-G

45395612-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122457380-T-G

45395632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122457400-A-G

http://identifiers.org/hco/15/GRCh38#45395805-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122457558-A-C

45396003-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122457715-G-C

45396025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122457737-G-T

45399653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122459550-A-G

http://identifiers.org/hco/15/GRCh38#45399673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122459573-C-A

45399673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122459573-C-T

45399739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122459635-G-A

http://identifiers.org/hco/15/GRCh38#45399805-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#122459698-A-C

45399874-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122459761-G-C

45400445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122460306-T-C

45400766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122460663-T-C

45400859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122460756-A-G

45402228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: non coding transcript exon variant
orthologous variants: 122461007-G-A

45402228-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: non coding transcript exon variant
orthologous variants: 122461007-G-C

45402228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: non coding transcript exon variant
orthologous variants: 122461007-G-T

http://identifiers.org/hco/15/GRCh38#45402258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#122461035-C-A

45402258-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 122461035-C-G

45402258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 122461035-C-T

45402263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 122461039-T-C

45402263-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 122461039-T-G

45402291-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: non coding transcript exon variant
orthologous variants: 122461067-T-A

45402291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: non coding transcript exon variant
orthologous variants: 122461067-T-C

http://identifiers.org/hco/15/GRCh38#45402321-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122461090-C-A

45402321-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: non coding transcript exon variant
orthologous variants: 122461090-C-G

45402321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4175
most severe consequence: non coding transcript exon variant
orthologous variants: 122461090-C-T