http://identifiers.org/hco/6/GRCh38#41546436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48235530-C-A

41546436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48235530-C-T

41546440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48235526-C-T

http://identifiers.org/hco/6/GRCh38#41546623-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48235349-A-C

41546623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48235349-A-G

41546688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48235282-T-C

41546688-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48235282-T-G

41546692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48235278-G-T

41546861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48235135-G-A

41546861-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48235135-G-C

41546861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48235135-G-T

41546963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48235029-T-C

41547001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48234991-G-A

41547063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48234937-C-T

41547096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48234904-T-C

41547380-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48234611-C-G

41547380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48234611-C-T

http://identifiers.org/hco/6/GRCh38#41547399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48234592-C-A

41547399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48234592-C-T

41547427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48234567-A-G

41547427-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48234567-A-T

http://identifiers.org/hco/6/GRCh38#41547511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48234485-C-A

41547511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48234485-C-T

41547620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48234367-T-C

41547637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48234320-A-G

41547658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48234299-T-C

http://identifiers.org/hco/6/GRCh38#41547822-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48234131-A-C

41548012-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48233898-T-A

41548021-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48233889-C-G

http://identifiers.org/hco/6/GRCh38#41548187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48233698-C-A

41548187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48233698-C-T

41548215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48233670-G-A

41548382-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48233495-A-T

41548429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48233445-C-T

http://identifiers.org/hco/6/GRCh38#41548586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48233290-C-A

41548586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48233290-C-T

41548649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 48233237-T-C

http://identifiers.org/hco/6/GRCh38#41548701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#48233205-C-A

41548704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 48233202-G-A

41548908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48232977-T-C

41549058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48232867-C-T

41549061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48232864-C-T

41549665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48232195-A-G

41549694-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48232166-T-G

41549702-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48232158-T-G

41549744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48232130-G-A

41549765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48232114-A-G

41549787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48232092-G-A

41550154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48231743-C-T

41550409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48231471-A-G

41550515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48231363-A-G

41550821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48231099-C-T

41550850-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48231062-T-G

41550947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48230972-G-T

41550953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48230966-A-G

41551024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48230889-G-T

41551358-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48230603-C-G

41551483-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48230468-C-G

41551501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48230450-G-A

41551788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48230124-C-T

41551908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48230018-T-C

http://identifiers.org/hco/6/GRCh38#41552033-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48229902-C-A

41552033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48229902-C-T

41552040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48229896-C-T

41552059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48229869-G-A

41552059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48229869-G-T

41552061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48229867-G-A

41552101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48229826-G-A

41552101-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48229826-G-T

41552118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48229809-G-A

41552164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48229749-G-A

41552279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48229656-G-T

41552377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48229546-C-T

41552436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48229344-T-C

41552436-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48229344-T-G

http://identifiers.org/hco/6/GRCh38#41552450-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48229329-A-C

41552450-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48229329-A-T

41552873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48229022-C-T

41552888-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48229009-T-G

41552889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48229008-G-A

41553090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48228858-G-A

41553159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48228787-A-G

http://identifiers.org/hco/6/GRCh38#41553385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48228560-C-A

41553385-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48228560-C-G

41553385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48228560-C-T

41553419-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48228524-C-G

41553639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48228319-C-T

41553753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48228095-C-T

41553938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48227871-G-A

41554066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48227648-G-A

41554169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48227531-C-T

41554193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48227507-G-A

41554193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48227507-G-T

41554205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48227494-A-G

41554342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48227347-T-C

41554408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48227293-G-A

41554452-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48227265-C-G

41554452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48227265-C-T

41556147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48225495-G-A

41556259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48225415-G-A

41556854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48224527-A-G

41556875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48224506-C-T

41556974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48224419-T-C

41557262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48224165-G-A

41558080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48222767-C-T

41558118-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48222736-G-C

41558270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48222611-C-T

41558444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48222484-T-C

41558450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48222478-C-T

41558495-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48222433-T-A

41558521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48222407-G-A

41558793-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48222173-G-C

41558925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48222046-G-A

41559060-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48221916-T-G

41559391-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48221515-T-A

41559528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48221414-A-G

41559644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48221345-T-C

41560357-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48220924-C-G

http://identifiers.org/hco/6/GRCh38#41560562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48220797-C-A

http://identifiers.org/hco/6/GRCh38#41560569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48220788-C-A

41560569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48220788-C-T

41560572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48220785-G-A

41560572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48220785-G-T

41560579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48220774-G-A

http://identifiers.org/hco/6/GRCh38#41560927-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48220423-A-C

41560934-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48220416-C-G

http://identifiers.org/hco/6/GRCh38#41561206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48220149-C-A

41561206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48220149-C-T

41561451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48219776-C-T

http://identifiers.org/hco/6/GRCh38#41561492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48219742-C-A

41562157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48219109-G-T

41562487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48218768-A-G

41562496-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48218759-C-G

41562496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48218759-C-T

41562632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48218617-A-G

http://identifiers.org/hco/6/GRCh38#41563162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48218083-C-A

41563162-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48218083-C-G

41563220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48218029-G-A

41563276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48217968-A-G

41563297-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48217947-A-T

41563366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48217900-A-G

41563605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48217768-A-G

41563631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48217743-G-A

41563697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48217677-T-C

41563698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48217676-G-A

41563698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48217676-G-T

41563994-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48217611-G-C

http://identifiers.org/hco/6/GRCh38#41565694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48215502-C-A

41565724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48215472-G-A

41565724-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48215472-G-C

41565724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48215472-G-T

http://identifiers.org/hco/6/GRCh38#41565751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48215451-C-A

http://identifiers.org/hco/6/GRCh38#41565759-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48215443-A-C

41565782-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 48215419-G-C

41565875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 48215317-G-A

41566069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48215132-C-T

http://identifiers.org/hco/6/GRCh38#41566099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48215102-C-A

41566357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48214867-G-A

41566357-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48214867-G-T

41566611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48214319-A-G

41566679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48214256-A-G

http://identifiers.org/hco/6/GRCh38#41566735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48214204-C-A

41567007-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48214034-T-G

41567073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48213985-C-T

41567729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48212392-A-G

41567739-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48212382-C-G

41567944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48212176-G-A

41568045-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48212061-A-T

41568057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48212049-G-A

41568057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48212049-G-T

41568103-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48212009-T-G

41568120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48211999-T-C

41568295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48211842-C-T

41568436-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48211749-C-G

41568601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48210541-G-A

41568613-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48210528-G-C

41568660-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 48210487-G-C

41568661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 48210486-A-G

41568939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 48210249-A-G

http://identifiers.org/hco/6/GRCh38#41569110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48210115-C-A

41569167-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48210053-T-G

41569277-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48209956-C-G

41569288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48209943-G-A

41569785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48209516-G-A

41569923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48209373-A-G

41570032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48209279-G-A

41570032-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48209279-G-T

http://identifiers.org/hco/6/GRCh38#41570113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48209233-C-A

41570259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48209087-C-T

41570359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48209031-G-A

41570404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48208993-G-T

41571008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48208623-T-C

http://identifiers.org/hco/6/GRCh38#41571502-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48208302-A-C

41571618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48208197-C-T

http://identifiers.org/hco/6/GRCh38#41571752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48208011-C-A

41571752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48208011-C-T

41571826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48207904-C-T

41571831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48207899-G-T

41571880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48207863-G-A

41571993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48207784-A-G

41572002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48207775-A-G

41572002-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48207775-A-T

41572680-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48205807-C-G

41572698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48205789-G-A

41572747-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48205743-C-G

41573120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48205427-C-T

http://identifiers.org/hco/6/GRCh38#41573255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48205276-C-A

41573284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48205170-G-T

41573394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48205036-C-T

http://identifiers.org/hco/6/GRCh38#41573397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48205033-C-A

41573402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48205028-C-T

41573658-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48204831-G-C

41573672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48204817-G-A

41573766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48204721-G-A

41573855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48204636-A-G

41573942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48203815-T-C

41573948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48203809-G-A

41574454-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48202996-A-T

41574467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48202989-G-A

41574513-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48202944-T-G

41574610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48202862-T-C

41574618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48202639-G-T

41575451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48201633-G-A

41575540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48201575-G-A

41575540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48201575-G-T

41575733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48201423-C-T

41575757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48201386-C-T

41575785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48201360-G-A

41575904-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48201256-G-C

41575928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48201239-T-C

41575959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48201205-G-A

http://identifiers.org/hco/6/GRCh38#41576054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48201123-C-A

41576054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48201123-C-T

http://identifiers.org/hco/6/GRCh38#41576056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48201121-C-A

41576056-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48201121-C-G

41576351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48200857-T-C

41576420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48200783-T-C

41576570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48200522-C-T

http://identifiers.org/hco/6/GRCh38#41576694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48200423-C-A

41576998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48200102-G-A

41577609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48199625-C-T

41577788-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48199372-C-G

http://identifiers.org/hco/6/GRCh38#41577838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48199325-C-A

41577846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48199317-C-T

41577859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48199304-G-A

41577859-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48199304-G-C

41577859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48199304-G-T

http://identifiers.org/hco/6/GRCh38#41577871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48199291-C-A

41577871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48199291-C-T

http://identifiers.org/hco/6/GRCh38#41577878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48199284-C-A

41577878-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48199284-C-G

41577880-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48199282-T-A

41577898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48199262-T-C

http://identifiers.org/hco/6/GRCh38#41577933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48199209-C-A

http://identifiers.org/hco/6/GRCh38#41578137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48198993-C-A

41578137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48198993-C-T

41578143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48198987-G-A

41578143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48198987-G-T

http://identifiers.org/hco/6/GRCh38#41578181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48198931-C-A

41578232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48198891-G-A

41578232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48198891-G-T

41578339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48198817-C-T

41578344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48198812-C-T

http://identifiers.org/hco/6/GRCh38#41578699-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48198528-A-C

41578699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48198528-A-G

41578776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48198460-A-G

41578779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48198457-G-T

41578882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48198363-G-A

41578882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48198363-G-T

41579286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48197960-A-G

41579559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48197752-C-T

41581613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48195166-G-T

41581628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48195156-A-G

http://identifiers.org/hco/6/GRCh38#41581697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48195116-C-A

41581697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48195116-C-T

41581740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48195081-A-G

41581786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48195050-C-T

41581805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48195031-G-A

41583729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48193036-A-G

http://identifiers.org/hco/6/GRCh38#41583826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48192947-C-A

41583879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48192899-C-T

41584139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48192748-G-A

41584187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48192695-G-T

41584189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48192693-C-T

41584292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48192591-C-T

41584302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48192581-T-C

41584456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48192372-C-T

http://identifiers.org/hco/6/GRCh38#41584648-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48191915-A-C

41584648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48191915-A-G

41584649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48191914-G-T

http://identifiers.org/hco/6/GRCh38#41584667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48191896-C-A

41584667-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48191896-C-G

41584667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48191896-C-T

http://identifiers.org/hco/6/GRCh38#41584689-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48191870-A-C

41584689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48191870-A-G

41584800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 48191784-A-G

http://identifiers.org/hco/6/GRCh38#41584905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48191679-C-A

41584905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48191679-C-T

http://identifiers.org/hco/6/GRCh38#41584928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48191651-C-A

41584928-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48191651-C-G

41584928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48191651-C-T

41584933-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48191646-T-A

41584933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48191646-T-C

41584943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48191636-C-T

41584949-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48191630-A-T

41584960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48191613-A-G

http://identifiers.org/hco/6/GRCh38#41585019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48191549-C-A

41585019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48191549-C-T

41585068-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48191524-A-T

41585078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48191519-T-C

41585080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48191517-C-T

41585250-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48191380-T-G

41585313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48191330-G-T

http://identifiers.org/hco/6/GRCh38#41585320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48191323-C-A

41585320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48191323-C-T

41585356-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48191307-A-T

41585420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48191283-C-T

41585550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48191150-T-C

41585578-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48191110-G-C

41585616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48191070-A-G

41585668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48191017-G-T

41585789-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48190907-G-T

41585810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48190886-G-A

http://identifiers.org/hco/6/GRCh38#41585946-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48190768-A-C

41586119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48190616-C-T

41586206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48190525-G-T

41586399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48190342-G-A

41586457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48190290-G-A

http://identifiers.org/hco/6/GRCh38#41586897-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48189789-A-C

41586897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48189789-A-G

41586955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48189731-A-G

41586955-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48189731-A-T

http://identifiers.org/hco/6/GRCh38#41586958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48189728-C-A

41586958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48189728-C-T

41587272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 48189450-T-C

41587272-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 48189450-T-G

41587395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 48189324-T-C

41587467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 48189252-C-T

41587546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48189172-G-T

41587557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48189161-G-T

41587602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48189093-G-A

41587602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48189093-G-T

41587613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48189082-C-T

41587691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48189034-G-T

http://identifiers.org/hco/6/GRCh38#41587718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48189018-C-A

41587718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48189018-C-T

41587728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48189009-G-A

41587728-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48189009-G-C

http://identifiers.org/hco/6/GRCh38#41587729-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48189008-C-A

41587745-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48188992-T-A

41587745-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48188992-T-G

41587815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 48188933-G-A

41587815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 48188933-G-T

41587983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48188789-G-A

41588014-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48188750-T-A

41588014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48188750-T-C

http://identifiers.org/hco/6/GRCh38#41588508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48188299-C-A

41588598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48188200-A-G

http://identifiers.org/hco/6/GRCh38#41588829-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48188035-A-C

41588829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48188035-A-G

41588829-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48188035-A-T

41588863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48188003-T-C

http://identifiers.org/hco/6/GRCh38#41588876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48187990-C-A

41588876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48187990-C-T

41588886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48187980-T-C

41589378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48187592-C-T

41589655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48187330-G-A

41589655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48187330-G-T

41589665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48187325-G-A

41589665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48187325-G-T

41589748-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48186867-T-A

41589748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48186867-T-C

41589787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 48186830-A-G

41589859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48186758-G-A

http://identifiers.org/hco/6/GRCh38#41589878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48186736-C-A

41589878-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48186736-C-G

41589878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48186736-C-T

http://identifiers.org/hco/6/GRCh38#41589909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48186701-C-A

41589909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48186701-C-T

41589917-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48186693-C-G

41589917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48186693-C-T

41589944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48186666-C-T

http://identifiers.org/hco/6/GRCh38#41590192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48186430-C-A

41590192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48186430-C-T

41590257-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48186369-G-C

http://identifiers.org/hco/6/GRCh38#41590312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48186313-C-A

41590312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 48186313-C-T

41590330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 48186295-G-A

41590392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48186236-T-C

41590443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48186213-A-G

41590495-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48186172-T-A

41590495-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48186172-T-G

41590560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48186128-G-A

41590618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48186073-A-G

41590828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48185974-G-A

41591112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48185753-A-G

41591185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48185695-A-G

41591185-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48185695-A-T

41591308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 48185572-A-G

41591327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48185553-A-G

41591345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48185532-T-C

41591368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48185514-C-T

41591459-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48185429-G-C

http://identifiers.org/hco/6/GRCh38#41591470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48185420-C-A

http://identifiers.org/hco/6/GRCh38#41591471-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48185419-A-C

41591471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48185419-A-G

41591984-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48184778-A-T

41592052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48184700-A-G

http://identifiers.org/hco/6/GRCh38#41592123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48184628-C-A

41592403-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 48184346-G-C

41592481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 48184268-G-A

41592605-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron variant
orthologous variants: 48184170-G-C

41593182-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron variant
orthologous variants: 48183897-C-G

41593284-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron variant
orthologous variants: 48183810-C-G

41593402-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron variant
orthologous variants: 48183696-C-G

41593417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron variant
orthologous variants: 48183682-C-T

41593555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron variant
orthologous variants: 48183543-G-A

41593555-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron variant
orthologous variants: 48183543-G-C

41593597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron variant
orthologous variants: 48183501-A-G

41593599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron variant
orthologous variants: 48183499-C-T

41594093-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron variant
orthologous variants: 48183037-G-C

41594165-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron variant
orthologous variants: 48182969-A-T

41594184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron variant
orthologous variants: 48182950-G-A

41594302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron variant
orthologous variants: 48182835-T-C

41594366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron variant
orthologous variants: 48182767-G-A

41594530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron variant
orthologous variants: 48182617-A-G

41594644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron variant
orthologous variants: 48182547-T-C

http://identifiers.org/hco/6/GRCh38#41594751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48182393-C-A

41594751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron variant
orthologous variants: 48182393-C-T

41594789-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron variant
orthologous variants: 48182354-G-C

41594789-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron variant
orthologous variants: 48182354-G-T

41594818-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron variant
orthologous variants: 48182317-T-G

http://identifiers.org/hco/6/GRCh38#41594829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48182306-C-A

41594829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron variant
orthologous variants: 48182306-C-T

41594831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron variant
orthologous variants: 48182304-A-G

41594833-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron variant
orthologous variants: 48182302-C-G

41595012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron variant
orthologous variants: 48182133-A-G

http://identifiers.org/hco/6/GRCh38#41595042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48182107-C-A

41595056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron variant
orthologous variants: 48182099-C-T

http://identifiers.org/hco/6/GRCh38#41595085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48182078-C-A

41595085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron variant
orthologous variants: 48182078-C-T

41595104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron variant
orthologous variants: 48182063-G-A

41595121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron variant
orthologous variants: 48182046-G-A

41595121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron variant
orthologous variants: 48182046-G-T

41595125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron variant
orthologous variants: 48182042-G-A

41595125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron variant
orthologous variants: 48182042-G-T

41595455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron variant
orthologous variants: 48181767-G-A

41597156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron variant
orthologous variants: 48180732-T-C

41597271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron variant
orthologous variants: 48180626-C-T

http://identifiers.org/hco/6/GRCh38#41597335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48180591-C-A

41597335-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron variant
orthologous variants: 48180591-C-G

41597390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron variant
orthologous variants: 48180548-C-T

41597395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron variant
orthologous variants: 48180543-C-T

41597403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron variant
orthologous variants: 48180534-G-A

41597451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron variant
orthologous variants: 48180486-G-A

41597916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: missense variant
orthologous variants: 48180061-A-G

http://identifiers.org/hco/6/GRCh38#41597922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48180055-C-A

41597922-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: missense variant
orthologous variants: 48180055-C-G

41597922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: missense variant
orthologous variants: 48180055-C-T

41598063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron variant
orthologous variants: 48179999-C-T

41598109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron variant
orthologous variants: 48179967-C-T

41598122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron variant
orthologous variants: 48179949-C-T

41598154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron variant
orthologous variants: 48179917-C-T

41598155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron variant
orthologous variants: 48179916-C-T

41598218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: intron variant
orthologous variants: 48179859-T-C

41598929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: missense variant
orthologous variants: 48179586-T-C

http://identifiers.org/hco/6/GRCh38#41599060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48179460-C-A

41599060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 3 prime UTR variant
orthologous variants: 48179460-C-T

41599297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 3 prime UTR variant
orthologous variants: 48179225-G-A

41599297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 3 prime UTR variant
orthologous variants: 48179225-G-T

41599448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 3 prime UTR variant
orthologous variants: 48179073-G-A

41599448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 3 prime UTR variant
orthologous variants: 48179073-G-T

41599506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 3 prime UTR variant
orthologous variants: 48179022-T-C

41599507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 3 prime UTR variant
orthologous variants: 48179021-G-A

41599507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 3 prime UTR variant
orthologous variants: 48179021-G-T

41599513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 3 prime UTR variant
orthologous variants: 48179015-G-A

41599513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 3 prime UTR variant
orthologous variants: 48179015-G-T

41599516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 3 prime UTR variant
orthologous variants: 48179012-G-T

41599598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 3 prime UTR variant
orthologous variants: 48178964-G-A

41599598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 3 prime UTR variant
orthologous variants: 48178964-G-T

41599607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 3 prime UTR variant
orthologous variants: 48178955-G-T

http://identifiers.org/hco/6/GRCh38#41599798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48178816-C-A

41599812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 3 prime UTR variant
orthologous variants: 48178802-G-A

41599812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 3 prime UTR variant
orthologous variants: 48178802-G-T

http://identifiers.org/hco/6/GRCh38#41600021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48178628-C-A

41600028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 3 prime UTR variant
orthologous variants: 48178621-C-T

http://identifiers.org/hco/6/GRCh38#41600029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48178620-C-A

http://identifiers.org/hco/6/GRCh38#41600178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48178489-C-A

http://identifiers.org/hco/6/GRCh38#41600241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48178462-C-A

41600241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 3 prime UTR variant
orthologous variants: 48178462-C-T

41600258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 3 prime UTR variant
orthologous variants: 48178448-G-A

41600258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 3 prime UTR variant
orthologous variants: 48178448-G-T

41600309-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 3 prime UTR variant
orthologous variants: 48178388-C-G

41600334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 3 prime UTR variant
orthologous variants: 48178363-G-A

41600334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 3 prime UTR variant
orthologous variants: 48178363-G-T

41600364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 3 prime UTR variant
orthologous variants: 48178333-A-G

41600413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 3 prime UTR variant
orthologous variants: 48178287-G-A

41600413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 3 prime UTR variant
orthologous variants: 48178287-G-T

http://identifiers.org/hco/6/GRCh38#41600414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48178286-C-A

41600414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 3 prime UTR variant
orthologous variants: 48178286-C-T

http://identifiers.org/hco/6/GRCh38#41600416-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48178284-A-C

41600509-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 3 prime UTR variant
orthologous variants: 48178195-A-T

41600543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 3 prime UTR variant
orthologous variants: 48178143-G-A

http://identifiers.org/hco/6/GRCh38#41600582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#48178099-C-A

41600660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 3 prime UTR variant
orthologous variants: 48178022-G-A

41600660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20842
most severe consequence: 3 prime UTR variant
orthologous variants: 48178022-G-T