87627613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 8673770-G-A

87627613-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 8673770-G-C

http://identifiers.org/hco/7/GRCh38#87627675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8673716-C-A

87627718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8673673-G-A

http://identifiers.org/hco/7/GRCh38#87627904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8673523-C-A

87627904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8673523-C-T

http://identifiers.org/hco/7/GRCh38#87627906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8673521-C-A

87628164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8673277-C-T

87628192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8673249-C-T

87628212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8673233-G-A

87628312-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8673137-T-G

87628341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8673108-G-T

http://identifiers.org/hco/7/GRCh38#87628357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#8673092-C-A

87628393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8673050-G-A

http://identifiers.org/hco/7/GRCh38#87628402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#8673041-C-A

87628402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8673041-C-T

87628508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 8672948-G-A

http://identifiers.org/hco/7/GRCh38#87628527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#8672928-C-A

87628545-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8672898-A-T

87628552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8672892-G-A

87628552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8672892-G-T

87628615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8672818-G-A

http://identifiers.org/hco/7/GRCh38#87628693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8672741-C-A

87628693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8672741-C-T

http://identifiers.org/hco/7/GRCh38#87628734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8672693-C-A

87628734-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8672693-C-G

87628734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8672693-C-T

http://identifiers.org/hco/7/GRCh38#87628819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8672615-C-A

87628819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8672615-C-T

87628864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8672567-G-A

87628864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8672567-G-T

87628899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8672532-G-A

87628899-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8672532-G-C

87628899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8672532-G-T

87629039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 8672452-G-A

87629168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 8672321-T-C

http://identifiers.org/hco/7/GRCh38#87629218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8672275-C-A

87629218-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 8672275-C-G

87629218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 8672275-C-T

87629232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8672261-A-G

87629970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8671958-A-G

87632387-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8670720-T-G

87632441-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8670670-T-G

87632708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8670276-G-A

87632734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8670249-G-T

87635227-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8668189-T-G

87635271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8668153-A-G

87635503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8667927-C-T

87646683-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8655169-T-A

87650690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8654094-G-T

87650700-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8654084-A-T

http://identifiers.org/hco/7/GRCh38#87650802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8654015-C-A

87650802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8654015-C-T

http://identifiers.org/hco/7/GRCh38#87650945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8653860-C-A

87650945-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 8653860-C-G

87650945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 8653860-C-T

http://identifiers.org/hco/7/GRCh38#87651040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8652097-C-A

87651083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8652026-A-G

87651501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8651436-G-A

87651501-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8651436-G-C

http://identifiers.org/hco/7/GRCh38#87651535-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8651410-A-C

87651593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8651353-A-G

87651762-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8651194-A-T

87651824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8651154-T-C

87651933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8651051-T-C

87652111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8645587-T-C

87652478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8645251-G-T

87652727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8644924-T-C

87652844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8644806-G-A

87652844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8644806-G-T

87653229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8644407-G-A

http://identifiers.org/hco/7/GRCh38#87686149-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8641861-A-C

87686259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8641759-T-C

87687074-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8641326-A-T

87687499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8640957-G-A

87687751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8640730-T-C

87688175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8640315-A-G

http://identifiers.org/hco/7/GRCh38#87690278-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8636498-A-C

87691706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8630846-A-G

87691963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8630625-T-C

87692071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8630522-A-G

87693068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8629979-C-T

87693112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8629935-T-C

87693123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8629924-T-C

87693308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8629580-A-G

87693469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8629424-A-G

87693527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8629373-A-G

87700402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8629175-C-T

87700660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8628742-A-G

87700661-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8628741-G-T

87700877-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8628575-T-A

87700970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8628503-T-C

87700970-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8628503-T-G

87701010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8628473-C-T

87703037-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8626459-T-G

87707535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8623430-G-A

87707555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8623410-C-T

87707691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8623253-A-G

87708105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8622823-T-C

87708202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8622737-A-G

http://identifiers.org/hco/7/GRCh38#87708342-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8622436-A-C

87708342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8622436-A-G

87708348-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8622402-G-C

http://identifiers.org/hco/7/GRCh38#87708381-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8622374-A-C

87708708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8622080-T-C

87708943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8621871-C-T

87708963-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8621856-T-G

87709136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8621684-T-C

87709141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8621679-A-G

87709197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8621622-T-C

http://identifiers.org/hco/7/GRCh38#87709214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8621605-C-A

87709214-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8621605-C-G

87709249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8621572-T-C

87709411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8621397-G-T

87709431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8621378-A-G

87709432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8621377-C-T

87709524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8621291-G-A

87709524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8621291-G-T

87709654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8621209-T-C

87709654-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8621209-T-G

87709828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8621038-T-C

http://identifiers.org/hco/7/GRCh38#87709991-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8620074-A-C

87709991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8620074-A-G

87710161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8619906-T-C

87710337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8619791-C-T

http://identifiers.org/hco/7/GRCh38#87710439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8619696-C-A

87710664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8619484-G-A

87710664-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8619484-G-C

87710748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8619425-T-C

http://identifiers.org/hco/7/GRCh38#87710755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8619418-C-A

87710782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8619391-C-T

http://identifiers.org/hco/7/GRCh38#87710796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8619377-C-A

87710796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8619377-C-T

87710866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8619302-C-T

87710886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8619282-T-C

87710886-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8619282-T-G

87711444-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8619018-G-C

87711502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8618959-G-T

87711653-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8618802-A-T

http://identifiers.org/hco/7/GRCh38#87711669-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8618785-A-C

87711904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8618598-C-T

87711955-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8618547-G-C

87711962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8618540-T-C

87712020-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8618485-T-A

http://identifiers.org/hco/7/GRCh38#87712162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8618155-C-A

87712163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8618154-C-T

87712246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8618079-A-G

http://identifiers.org/hco/7/GRCh38#87712901-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8617484-A-C

87713325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8617069-T-C

87713392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8617012-C-T

87713417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8616986-A-G

87713520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8616885-G-A

87713520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8616885-G-T

87713648-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8616767-A-T

87713685-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8616746-G-C

87713792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8616641-A-G

87713972-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8616409-C-G

87735528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8613946-T-C

87735667-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8613777-C-G

87735887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8613565-A-G

87736102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8613256-T-C

87736310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8613059-A-G

87737232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8612675-C-T

87737765-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8612290-T-A

87737960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8612094-C-T

87739183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8610061-C-T

87739351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8609901-A-G

87739509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8609741-A-G

http://identifiers.org/hco/7/GRCh38#87739677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8609599-C-A

87739677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8609599-C-T

87739749-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8609540-T-A

87739765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8609525-A-G

87739765-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8609525-A-T

87739891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8609397-A-G

87739891-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8609397-A-T

87740161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8609217-G-A

87740482-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8608929-T-A

87740535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8608882-G-A

87741453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8598356-A-G

http://identifiers.org/hco/7/GRCh38#87741648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8598168-C-A

87741648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8598168-C-T

87749511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8594551-G-A

87749885-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8594306-T-A

87749946-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8594290-T-G

87749980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8594283-A-G

http://identifiers.org/hco/7/GRCh38#87770497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8578861-C-A

87770497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8578861-C-T

87770666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 8578687-C-T

87770851-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8578502-T-A

87770851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8578502-T-C

87777668-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8571148-T-A

87777668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8571148-T-C

87777786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8571026-C-T

87778014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8570801-G-A

87778014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8570801-G-T

87778042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8570773-G-A

87778042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8570773-G-T

87778067-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8570746-T-G

87778606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8570486-G-A

87778707-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8570390-T-G

http://identifiers.org/hco/7/GRCh38#87778800-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8570280-A-C

87778923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8570168-T-C

87778929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8570162-G-A

87779049-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8570053-G-C

87779227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8569867-T-C

http://identifiers.org/hco/7/GRCh38#87779361-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8569645-A-C

87779425-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8569598-A-T

87779576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8569438-C-T

87787066-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8567487-G-C

87804889-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8565361-T-G

87804947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8565308-A-G

87805185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8565130-A-G

87805226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8565089-A-G

87805238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8565077-T-C

http://identifiers.org/hco/7/GRCh38#87805545-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8564766-A-C

87805878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8564193-G-A

http://identifiers.org/hco/7/GRCh38#87806203-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8563890-A-C

87806210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8563876-T-C

87806285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8563807-T-C

87806914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8562852-G-A

87807231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8562561-A-G

87807236-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8562556-T-A

http://identifiers.org/hco/7/GRCh38#87807246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8562532-C-A

87807246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8562532-C-T

87807651-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8562100-A-T

87807763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8562010-G-A

87807763-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8562010-G-C

87808088-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8561766-A-T

87808746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8561090-A-G

87809072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8560044-G-A

87809079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8560037-A-G

87809079-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8560037-A-T

87809391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8559750-A-G

87809621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8559580-T-C

87810530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8558262-C-T

http://identifiers.org/hco/7/GRCh38#87810656-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8558147-A-C

87810686-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8558120-T-G

87810708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8558090-T-C

87810822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8557965-G-A

87811347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8557123-T-C

87811393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8557077-G-A

87811394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8557076-C-T

87811587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8556906-T-C

87811676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8556833-A-G

87811988-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8554998-G-C

87812111-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8554865-T-A

87812710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8554748-G-T

87812749-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8554701-T-G

87812769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8554679-G-A

http://identifiers.org/hco/7/GRCh38#87812978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8547768-C-A

87813171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8547591-C-T

87813190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8547571-A-G

87813316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8547463-G-A

http://identifiers.org/hco/7/GRCh38#87813516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8547300-C-A

87813564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8547265-A-G

87813569-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8547260-T-G

87814494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8546668-G-A

87814611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8546557-A-G

87814664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8546507-A-G

87814846-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8546343-T-G

87815271-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8545754-T-G

http://identifiers.org/hco/7/GRCh38#87816007-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8545031-A-C

87816007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8545031-A-G

87830059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8542415-T-C

87830127-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8542350-T-A

87830127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8542350-T-C

87830131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8542346-T-C

http://identifiers.org/hco/7/GRCh38#87830292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8542194-C-A

87830292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8542194-C-T

87830293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8542193-G-A

87830293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8542193-G-T

87830328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8542157-A-G

87830328-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8542157-A-T

87830345-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8542137-T-G

http://identifiers.org/hco/7/GRCh38#87830354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8542128-C-A

87830354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8542128-C-T

87831086-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8541515-T-A

87831440-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8541134-T-G

87831623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8540987-T-C

87831770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8540849-G-T

87832064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8540548-G-A

87832101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8540512-T-C

87832116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8540497-A-G

87832116-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8540497-A-T

87832194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30286
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8540434-C-T