49636786-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 99207014-G-C

49637031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99207217-G-A

49637031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99207217-G-T

49637178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99207334-G-A

49637178-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99207334-G-T

49637381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99207473-T-C

http://identifiers.org/hco/12/GRCh38#49637423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99207514-C-A

49637423-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99207514-C-G

49637429-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99207520-C-G

49637429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99207520-C-T

49637553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 99207649-T-C

49637613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99207709-G-A

http://identifiers.org/hco/12/GRCh38#49637835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#99207928-C-A

49637835-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99207928-C-G

http://identifiers.org/hco/12/GRCh38#49637916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#99208005-C-A

49638001-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 99208099-G-T

49638060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 99208211-T-C

http://identifiers.org/hco/12/GRCh38#49638134-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#99208285-A-C

49638134-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 99208285-A-T

49638166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 99208322-G-A

49638166-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 99208322-G-C

49638166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 99208322-G-T

49638182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 99208338-G-A

49638182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 99208338-G-T

49638223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 99208374-G-A

49638251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 99208429-G-A

49638439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 99208747-A-G

49638880-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99209381-A-T

49638881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99209382-G-T

49638938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99209479-G-A

49639031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 99209599-G-T

http://identifiers.org/hco/12/GRCh38#49639350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#99209736-C-A

49639593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99209907-G-T

49639769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99210535-G-A

49639769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99210535-G-T

49639977-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99210709-G-C

http://identifiers.org/hco/12/GRCh38#49640127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#99210821-C-A

49640127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99210821-C-T

49640421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99211031-G-T

http://identifiers.org/hco/12/GRCh38#49640631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#99211117-C-A

49640631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99211117-C-T

49640649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99211118-T-C

49640983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99211677-G-A

49640983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99211677-G-T

49641046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99211738-G-A

http://identifiers.org/hco/12/GRCh38#49641106-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#99211768-A-C

http://identifiers.org/hco/12/GRCh38#49641412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#99212025-C-A

49641515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99212112-G-T

49641718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99212289-G-A

49641718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99212289-G-T

49642747-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99213230-G-C

http://identifiers.org/hco/12/GRCh38#49642763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#99213242-C-A

49642763-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99213242-C-G

49642763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99213242-C-T

49642792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99213275-G-T

49643028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 99213462-T-C

49643085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 99213514-C-T

49643146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 99213546-C-T

49643202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 99213584-T-C

49643344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 99213725-G-A

49643344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 99213725-G-T

49643424-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 99213808-C-G

49643424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 99213808-C-T

http://identifiers.org/hco/12/GRCh38#49643506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#99213875-C-A

49643506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 99213875-C-T

49643769-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 99214044-C-G

49643769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 99214044-C-T

49643839-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99214102-G-C

49644114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, missense_variant, synonymous_variant
orthologous variants: 99214356-G-A

49644245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3 prime UTR variant
orthologous variants: 99214486-C-T

49645027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 99215169-C-T

49645282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 99215668-G-A

49645282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 99215668-G-T

49645302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 99215688-T-C

http://identifiers.org/hco/12/GRCh38#49645319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99215705-C-A

49645369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 99215732-G-A

49645369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 99215732-G-T

http://identifiers.org/hco/12/GRCh38#49645420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99215783-C-A

49645447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 99215810-G-A

49645447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 99215810-G-T

http://identifiers.org/hco/12/GRCh38#49645641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99216011-C-A

49645675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 99216042-A-G

http://identifiers.org/hco/12/GRCh38#49645677-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99216044-A-C

49645677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 99216044-A-G

49645902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 99216252-G-A

49645902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 99216252-G-T

49645920-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99216270-A-T

49645934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99216288-G-T

http://identifiers.org/hco/12/GRCh38#49645987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99216315-C-A

49645987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99216315-C-T

49646011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99216338-G-T

49646031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99216359-A-G

49646218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99216474-A-G

49647016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 99217141-C-T

49647111-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99217246-G-C

49647111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99217246-G-T

49647144-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99217280-T-G

49647145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99217281-C-T

49647427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99217595-G-A

49647427-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99217595-G-C

49647427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99217595-G-T

49647445-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99217614-A-T

49647459-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99217628-G-C

49647459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99217628-G-T

http://identifiers.org/hco/12/GRCh38#49647555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99217725-C-A

49647555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99217725-C-T

49647874-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99218012-G-C

49647877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99218015-G-A

49647877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99218015-G-T

49648072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99218134-T-C

49648264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 99218305-C-T

49648340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 99218381-G-A

49648340-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 99218381-G-C

49648369-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99218410-C-G

http://identifiers.org/hco/12/GRCh38#49648408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99218434-C-A

http://identifiers.org/hco/12/GRCh38#49648947-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99218864-A-C

http://identifiers.org/hco/12/GRCh38#49649138-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99219026-A-C

http://identifiers.org/hco/12/GRCh38#49649178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99219064-C-A

49649178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99219064-C-T

49649179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99219065-G-A

49649261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 99219138-G-A

49649427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99219275-G-A

49649427-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99219275-G-C

49649500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 99219345-C-T

49649560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99219405-G-A

49649572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99219415-G-A

49650640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99220040-G-T

49650652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99220052-G-A

49651163-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99220479-G-C

49651301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99220619-G-A

49651425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 99220736-G-A

49651473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99220782-A-G

http://identifiers.org/hco/12/GRCh38#49651812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99221087-C-A

49651812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99221087-C-T

49651825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99221100-A-G

49651844-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99221118-G-C

49651844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99221118-G-T

49651950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 99221218-G-T

49652017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 99221285-C-T

49652172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 99221440-C-T

49653131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99222507-T-C

49653316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: synonymous variant
orthologous variants: 99222712-C-T

49653344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99222740-G-A

49653451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99222835-G-A

49653451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99222835-G-T

49653544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99222945-C-T

49653563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99222965-T-C

49653788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: synonymous variant
orthologous variants: 99223185-C-T

49653791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: synonymous variant
orthologous variants: 99223188-C-T

49653854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: synonymous variant
orthologous variants: 99223251-G-A

49653854-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: missense variant
orthologous variants: 99223251-G-C

49653915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99223307-G-T

49653974-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99223356-T-G

49654076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99223411-G-T

http://identifiers.org/hco/12/GRCh38#49654886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99223711-C-A

49654886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99223711-C-T

49654937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: synonymous variant
orthologous variants: 99223762-C-T

http://identifiers.org/hco/12/GRCh38#49654996-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99223821-A-C

49654996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99223821-A-G

http://identifiers.org/hco/12/GRCh38#49655040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99223865-C-A

49655040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99223865-C-T

49655090-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99223915-G-C

49655090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99223915-G-T

49655484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99224197-C-T

49655572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99224269-T-C

http://identifiers.org/hco/12/GRCh38#49655884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99224564-C-A

http://identifiers.org/hco/12/GRCh38#49656287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99225260-C-A

49656287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99225260-C-T

49656325-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99225285-G-C

49656325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99225285-G-T

http://identifiers.org/hco/12/GRCh38#49656354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99225309-C-A

49656354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99225309-C-T

http://identifiers.org/hco/12/GRCh38#49656386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99225374-C-A

49656386-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99225374-C-G

49656386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99225374-C-T

49656949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99225825-A-G

49657061-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99225919-T-A

http://identifiers.org/hco/12/GRCh38#49657327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99226163-C-A

49657327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99226163-C-T

49657742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99226544-C-T

49658007-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99226779-G-C

49658130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99226882-C-T

49658154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99226904-A-G

49658374-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99227096-T-A

49658374-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99227096-T-G

49658435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 99227154-C-T

49658450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 99227169-A-G

49658450-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 99227169-A-T

http://identifiers.org/hco/12/GRCh38#49658459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99227178-C-A

49658459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 99227178-C-T

49658471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 99227190-G-A

49658507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 99227226-T-C

49658507-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 99227226-T-G

49658522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 99227241-G-A

49658555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 99227274-T-C

49658603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99227322-T-C

49658701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99227423-A-G

49658730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99227452-A-G

49658738-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99227460-T-A

49658738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99227460-T-C

49658744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99227466-G-A

49658744-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99227466-G-C

49658744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99227466-G-T

49658788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99227506-C-T

49659603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99228061-G-A

49659654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99228088-A-G

49659654-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99228088-A-T

http://identifiers.org/hco/12/GRCh38#49660228-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99228453-C-A

http://identifiers.org/hco/12/GRCh38#49660244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99228463-C-A

49661067-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99228937-T-G

http://identifiers.org/hco/12/GRCh38#49661511-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99229313-A-C

49661729-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99229533-T-A

49661729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99229533-T-C

49661741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99229545-A-G

49661751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99229550-T-C

http://identifiers.org/hco/12/GRCh38#49661757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99229556-C-A

49661787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99229587-T-C

49661810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99229610-C-T

49661832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99229632-T-C

http://identifiers.org/hco/12/GRCh38#49662156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99230073-C-A

49662156-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99230073-C-G

49662156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99230073-C-T

http://identifiers.org/hco/12/GRCh38#49662195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99230112-C-A

49662195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99230112-C-T

http://identifiers.org/hco/12/GRCh38#49662196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99230113-C-A

49662299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99230186-C-T

49662830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99230637-A-G

49662860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99230675-A-G

49662944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99230764-G-A

http://identifiers.org/hco/12/GRCh38#49663385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99231180-C-A

49663385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99231180-C-T

49663440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99231233-G-T

49663655-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99231406-T-A

49663684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99231434-G-A

49664560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99231612-C-T

49664612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99231662-A-G

49664660-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99231701-C-G

49664925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99231973-C-T

49664955-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99232001-T-A

49665208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99232180-G-A

49665208-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99232180-G-C

49665267-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99232224-T-G

49665302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99232259-T-C

49665378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99232332-G-A

http://identifiers.org/hco/12/GRCh38#49665392-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99232346-A-C

49665837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 99232740-G-A

49666018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99233496-T-C

49666018-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99233496-T-G

49666035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99233513-A-G

49666260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99233697-G-A

49666260-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99233697-G-T

http://identifiers.org/hco/12/GRCh38#49666294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99233731-C-A

49666383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99233808-G-A

49666937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99234038-G-A

49666956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99234057-G-A

49667211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99234276-G-A

49667345-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99234390-C-G

49667406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99234432-T-C

49667474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99234491-T-C

49667891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99234826-G-A

http://identifiers.org/hco/12/GRCh38#49668657-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99235679-A-C

49668657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 99235679-A-G

49669181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 99236675-T-C

49669196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 99236690-A-G

49669269-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 99236763-T-G

49669385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 99236869-C-T

http://identifiers.org/hco/12/GRCh38#49669902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99237029-C-A

49670104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, undefined
orthologous variants: 99237153-C-T

49670264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99237274-C-T

49670312-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99237322-A-T

49670335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99237345-C-T

49670604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99237598-C-T

49671071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 99239152-G-A

49671168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99239249-C-T

49671183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 99239264-G-A

49671201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 99239283-C-T

49671365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 99239436-T-C

49671859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 99239862-G-A

49672041-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 99240017-T-A

http://identifiers.org/hco/12/GRCh38#49672224-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99240170-C-A

49672277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 99240222-T-C

49672289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 99240234-G-A

49672352-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 99240271-A-T

49672637-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 99240533-G-C

49672941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 99240840-C-T

49673404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 99241248-T-C

49673496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99241340-C-T

49673854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99241681-C-T

49674144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99241955-T-C

49674213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99241994-C-T

49674750-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99242512-C-G

49674817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99242579-T-C

49674894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99242656-T-C

49674894-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99242656-T-G

49674895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99242657-G-A

49675077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99242836-C-T

http://identifiers.org/hco/12/GRCh38#49675124-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99242883-A-C

49675215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99242963-T-C

49675294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99243041-A-G

49675396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99243143-A-G

49676035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99243756-C-T

49676134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99243824-G-A

49676261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99243914-C-T

49676466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99244100-T-C

49676508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99244401-G-T

49676531-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99244423-T-G

49676679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99244545-A-G

49677478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99245233-G-A

49677558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99245317-T-C

49677572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99245331-C-T

49677717-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99245468-T-G

49677767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99245518-A-G

49680046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99247846-T-C

http://identifiers.org/hco/12/GRCh38#49680072-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99247879-A-C

49680141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99247931-C-T

49680395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99248192-C-T

http://identifiers.org/hco/12/GRCh38#49681170-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99249798-A-C

49682961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99250338-A-G

49682981-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99250358-T-A

49683332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99250694-T-C

49683853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99251088-C-T

49683865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99251100-T-C

49684077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99251291-C-T

49684118-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99251332-G-C

http://identifiers.org/hco/12/GRCh38#49684267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99251462-C-A

http://identifiers.org/hco/12/GRCh38#49685884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99252964-C-A

49685884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99252964-C-T

49685933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99253014-G-A

49685974-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99253053-C-G

49685974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99253053-C-T

49686568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99253426-A-G

49686573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99253431-A-G

49686696-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99253546-G-C

49686757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99253600-G-A

49686790-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99253633-G-C

49686816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99253659-C-T

49687596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99253977-T-C

49688150-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99254482-T-A

49688258-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99254589-T-A

http://identifiers.org/hco/12/GRCh38#49688662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99254901-C-A

49688706-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99254944-G-T

49689163-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99255490-G-C

49689244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99255555-G-A

49689277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99255583-A-G

49689295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99255601-C-T

49689410-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99255723-C-G

49689499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99255793-T-C

49689563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99255817-C-T

49689564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99255818-C-T

49690254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99256461-T-C

49690277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99256484-G-T

49690351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99256512-T-C

49691018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99257055-G-A

49691237-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99257418-T-A

49692879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99258505-T-C

49695506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99259696-G-A

49696780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99260278-C-T

49696874-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99260353-G-C

http://identifiers.org/hco/12/GRCh38#49696906-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99260375-A-C

49697011-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99260468-G-C

49697090-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99260529-A-T

http://identifiers.org/hco/12/GRCh38#49697344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99260896-C-A

49697505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99260998-C-T

49697516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99261004-G-A

49697790-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99261331-C-G

http://identifiers.org/hco/12/GRCh38#49697844-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99261406-A-C

49697844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99261406-A-G

49698169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99261817-A-G

49698440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99262170-T-C

49698492-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99262217-G-C

http://identifiers.org/hco/12/GRCh38#49698983-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99262700-A-C

49699209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, undefined
orthologous variants: 99262874-G-A

49703673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99266802-A-G

49703735-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99266740-T-G

49703774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99266702-C-T

49703936-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99266529-T-A

49703951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99266514-T-C

49704059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99266413-G-A

49704067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99266405-T-C

49704087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99266385-G-A

http://identifiers.org/hco/12/GRCh38#49704127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99266345-C-A

49704582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99265839-G-A

49704608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99265814-G-A

49704614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99265808-A-G

49704644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99265777-G-A

49704644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99265777-G-T

http://identifiers.org/hco/12/GRCh38#49704738-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99265695-A-C

49705821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, missense_variant
orthologous variants: 99266995-T-C

49706053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99267224-T-C

49706275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 99267427-G-A

49706335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 99267489-T-C

49706373-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 99267535-G-C

http://identifiers.org/hco/12/GRCh38#49706593-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99267761-A-C

http://identifiers.org/hco/12/GRCh38#49706704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99267839-C-A

49706968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, undefined
orthologous variants: 99268005-G-A

49706968-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, undefined
orthologous variants: 99268005-G-C

49706968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, undefined
orthologous variants: 99268005-G-T

http://identifiers.org/hco/12/GRCh38#49707010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99268019-C-A

49707044-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron variant
orthologous variants: 99268047-T-A

49707120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 99268123-G-A

49707120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, missense_variant
orthologous variants: 99268123-G-T

49707348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99268326-G-A

49707348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99268326-G-T

49707649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: intron_variant, undefined
orthologous variants: 99268401-C-T

49707729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 99268481-G-A

49707729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 99268481-G-T

49707734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23698
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 99268487-C-T