http://identifiers.org/hco/2/GRCh38#227325213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#82702591-C-A

227325213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 82702591-C-T

http://identifiers.org/hco/2/GRCh38#227325259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#82702637-C-A

227325259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 82702637-C-T

227325281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 82702659-C-T

http://identifiers.org/hco/2/GRCh38#227325307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#82702684-C-A

227325307-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 82702684-C-G

227325307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 82702684-C-T

http://identifiers.org/hco/2/GRCh38#227325336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#82702713-C-A

227325336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 82702713-C-T

http://identifiers.org/hco/2/GRCh38#227325347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#82702724-C-A

227325347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 82702724-C-T

227325356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 82702733-A-G

http://identifiers.org/hco/2/GRCh38#227325368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#82702745-C-A

227325391-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 82702767-C-G

227325391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 82702767-C-T

http://identifiers.org/hco/2/GRCh38#227325411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#82702790-C-A

227325411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 82702790-C-T

http://identifiers.org/hco/2/GRCh38#227325512-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#82702873-A-C

227325522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82702880-G-A

227325522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82702880-G-T

227325567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82702901-C-T

227325569-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82702903-T-A

227325569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82702903-T-C

http://identifiers.org/hco/2/GRCh38#227325571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#82702905-C-A

227325571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82702905-C-T

http://identifiers.org/hco/2/GRCh38#227325573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#82702907-C-A

227325573-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82702907-C-G

227325573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82702907-C-T

http://identifiers.org/hco/2/GRCh38#227325577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#82702911-C-A

227325577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82702911-C-T

227325579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82702912-T-C

227325671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82702934-G-T

227325686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82702949-T-C

227325686-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82702949-T-G

227325787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82703065-G-T

http://identifiers.org/hco/2/GRCh38#227325798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#82703076-C-A

http://identifiers.org/hco/2/GRCh38#227325979-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#82703203-A-C

227326158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82703383-A-G

227326161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82703386-G-A

227326162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82703387-G-A

227326198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82703428-C-T

227326299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82703488-G-A

227326299-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82703488-G-C

227326314-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82703499-A-T

227327058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82704207-G-A

http://identifiers.org/hco/2/GRCh38#227327308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#82704442-C-A

227327308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82704442-C-T

227328579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82704859-G-A

http://identifiers.org/hco/2/GRCh38#227328580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#82704860-C-A

227328580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82704860-C-T

227328660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82704931-C-T

http://identifiers.org/hco/2/GRCh38#227328710-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#82704981-C-A

227328710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82704981-C-T

227328714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82704985-G-T

227328945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82705197-C-T

227328960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82705212-G-A

http://identifiers.org/hco/2/GRCh38#227329012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#82705299-C-A

227329300-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82705514-T-G

227329320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82705534-A-G

227329342-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82705555-T-A

227329342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82705555-T-C

227329383-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82705595-G-C

227329383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82705595-G-T

227329465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82705674-A-G

227329614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82705795-G-A

227329614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82705795-G-T

227329731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82705907-A-G

http://identifiers.org/hco/2/GRCh38#227330006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#82706268-C-A

227330006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82706268-C-T

227330012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82706275-G-T

http://identifiers.org/hco/2/GRCh38#227330254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#82706549-C-A

227330254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82706549-C-T

227330269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82706564-G-T

227330342-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82706673-T-G

http://identifiers.org/hco/2/GRCh38#227330408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#82706730-C-A

227330638-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 82706949-A-T

227330737-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 82707048-A-T

227330877-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82707187-T-A

227330894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82707204-A-G

227331219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82707638-C-T

227331288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82707736-C-T

227331506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82707994-T-C

227331736-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82708138-G-C

227331755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82708157-C-T

227332068-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82708459-T-G

227332513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 82708928-T-C

227332513-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 82708928-T-G

227332537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 82708952-A-G

227332549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 82708964-G-A

227332593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82709008-G-A

227332648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82709047-G-A

227332648-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82709047-G-C

http://identifiers.org/hco/2/GRCh38#227332659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#82709052-C-A

227332659-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82709052-C-G

227332659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82709052-C-T

227332675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82709067-G-A

227332675-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82709067-G-C

227332675-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82709067-G-T

227332905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82709408-A-G

227333079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82709570-G-A

227333099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82709590-C-T

227333395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82709815-G-A

227333630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82710044-G-A

227335897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82710490-G-A

http://identifiers.org/hco/2/GRCh38#227336024-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#82710613-A-C

227336060-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82710642-T-G

227336076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82710658-C-T

227336100-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82710687-T-G

227336167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82710737-G-A

227336203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82710770-T-C

227336336-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82710896-T-G

227336377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82710939-G-A

227336660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82711189-A-G

227336670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82711201-G-A

227337056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82711569-G-A

http://identifiers.org/hco/2/GRCh38#227340155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#82713000-C-A

227340155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82713000-C-T

227340165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82713010-T-C

227340176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82713021-T-C

227340176-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82713021-T-G

227340195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82713039-T-C

227340233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82713087-G-A

227340233-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82713087-G-T

227340247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82713101-A-G

227340282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82713130-G-A

227340282-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82713130-G-C

227340396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82713241-A-G

227340432-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82713272-T-G

227340872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82713417-G-A

227341060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82713512-G-A

227341197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82713620-A-G

227341222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82713626-A-G

227341238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82713642-C-T

227341288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82713691-G-T

227341305-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82713715-A-T

227341322-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82713726-A-T

227341758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82714124-A-G

227342297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82714448-A-G

227342625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82714612-G-A

227342625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82714612-G-T

http://identifiers.org/hco/2/GRCh38#227342798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#82714787-C-A

227342798-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82714787-C-G

227342798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82714787-C-T

http://identifiers.org/hco/2/GRCh38#227342810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#82714799-C-A

227342810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82714799-C-T

227342822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82714811-A-G

227342854-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82714845-T-A

227343049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82715018-G-A

227343053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82715022-A-G

227343203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82715166-C-T

227343285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82715271-G-A

227343381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82715369-A-G

227343771-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82715789-C-G

227343773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82715791-G-A

227343774-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82715792-G-C

227344112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82715992-T-C

227344139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82716014-G-A

227344405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82716262-G-A

227344415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82716271-A-G

227344711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82716503-A-G

227344822-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82716607-A-T

227344975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82716833-T-C

227346009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82718293-C-T

227346100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82718370-G-A

227346100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82718370-G-T

227346160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82718436-T-C

227346160-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82718436-T-G

http://identifiers.org/hco/2/GRCh38#227346232-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#82718571-A-C

227346232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82718571-A-G

227346259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82718656-A-G

227346548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82718949-A-G

227346745-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82719105-C-G

227346745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82719105-C-T

227346815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82719165-T-C

227346894-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82719233-T-G

http://identifiers.org/hco/2/GRCh38#227346930-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#82719276-C-A

227346930-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82719276-C-G

227346937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82719283-A-G

227346988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82719329-T-C

http://identifiers.org/hco/2/GRCh38#227347175-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#82719488-A-C

http://identifiers.org/hco/2/GRCh38#227347487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#82719797-C-A

227347744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82720059-G-A

227347886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82720185-C-T

227348247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82720513-T-C

227348577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82720835-T-C

227348691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82720944-A-G

227349081-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82721315-A-T

227349198-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82721392-T-A

http://identifiers.org/hco/2/GRCh38#227349289-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#82721492-A-C

227349384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82721584-C-T

227349530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82721886-G-T

227349565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82721932-G-A

227350352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82722671-C-T

227350472-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82722790-A-T

227350628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82722920-A-G

227350649-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82722941-C-G

227351270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82723564-T-C

http://identifiers.org/hco/2/GRCh38#227351821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#82724231-C-A

227351821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82724231-C-T

227351833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82724243-T-C

227351931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82724316-T-C

227351962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82724332-A-G

227351962-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82724332-A-T

http://identifiers.org/hco/2/GRCh38#227352172-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#82724524-C-A

227352172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82724524-C-T

227352456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82724749-A-G

227352456-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82724749-A-T

227352586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82724876-A-G

227352608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82724896-T-C

227352630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82724922-G-A

227352647-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82724942-T-G

http://identifiers.org/hco/2/GRCh38#227352654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#82724949-C-A

http://identifiers.org/hco/2/GRCh38#227352719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#82725016-C-A

227352719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82725016-C-T

227353137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82725443-T-C

227353458-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82725583-A-T

227353873-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82726325-G-C

227353908-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82726367-G-C

227353984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82726446-A-G

227354300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82726901-G-A

227354300-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82726901-G-C

227354330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82726934-G-A

227354548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82727146-G-T

227354597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82727194-G-A

227354918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82727479-T-C

http://identifiers.org/hco/2/GRCh38#227354988-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#82727617-C-A

227354988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82727617-C-T

227355193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82727828-A-G

227355199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82727834-G-T

http://identifiers.org/hco/2/GRCh38#227355360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#82727988-C-A

227355360-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82727988-C-G

227355360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82727988-C-T

227355373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82728001-G-T

227355402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82728027-G-A

227355402-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82728027-G-C

227355402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82728027-G-T

227355619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82728193-G-A

227355619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82728193-G-T

227355716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 82728280-G-A

227355716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 82728280-G-T

227355800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82728366-A-G

227355811-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82728377-A-T

227355878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82728446-A-G

227356242-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82728795-G-T

227356414-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82728847-G-C

227356497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82728880-G-A

http://identifiers.org/hco/2/GRCh38#227356854-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#82729187-A-C

227357009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 82729329-A-G

227357069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 82729389-T-C

227357110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82729430-G-A

227357113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82729433-G-A

http://identifiers.org/hco/2/GRCh38#227357136-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#82729456-A-C

http://identifiers.org/hco/2/GRCh38#227357207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#82729530-C-A

227357250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 82729559-G-A

227357250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 82729559-G-T

227357313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 82729612-G-A

227357313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 82729612-G-T

227357344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 82729640-A-G

227357344-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 82729640-A-T

227357420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 82729721-T-C

227357517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 82729816-C-T

http://identifiers.org/hco/2/GRCh38#227357565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#82729863-C-A

227357585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 82729883-T-C

227357585-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 82729883-T-G

227357594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 82729892-G-A

227357594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 82729892-G-T

227357601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 82729899-T-C

http://identifiers.org/hco/2/GRCh38#227357609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#82729903-C-A

http://identifiers.org/hco/2/GRCh38#227357633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#82729918-C-A

227357682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 82729975-T-C

227357685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 82729977-A-G

227357757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 82730038-G-T

227357758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24858
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 82730039-T-C