46052590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75521940-A-G

http://identifiers.org/hco/13/GRCh38#46052710-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#75521825-A-C

46052710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 75521825-A-G

46052739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 75521796-A-G

http://identifiers.org/hco/13/GRCh38#46052802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75521734-C-A

46052802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: non coding transcript exon variant
orthologous variants: 75521734-C-T

46052819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: non coding transcript exon variant
orthologous variants: 75521717-G-A

46052828-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: non coding transcript exon variant
orthologous variants: 75521707-C-G

46052849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: non coding transcript exon variant
orthologous variants: 75521692-T-C

46052849-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: non coding transcript exon variant
orthologous variants: 75521692-T-G

46052895-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: non coding transcript exon variant
orthologous variants: 75521653-C-G

46052934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: non coding transcript exon variant
orthologous variants: 75521621-G-A

http://identifiers.org/hco/13/GRCh38#46052947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75521608-C-A

46052947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: non coding transcript exon variant
orthologous variants: 75521608-C-T

http://identifiers.org/hco/13/GRCh38#46053005-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75521565-A-C

46053420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75521017-A-G

46053481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75520953-T-C

46053543-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75520918-T-A

46053543-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75520918-T-G

46053604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75520869-A-G

46053656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75520811-G-A

46055195-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75517449-A-T

46055325-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75517355-C-G

46055379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75517315-A-G

46055932-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75515479-A-T

46055934-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75515477-T-A

46055963-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75515448-T-A

46056370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75515063-A-G

46056557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75514903-T-C

46056670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75514322-T-C

46056997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75514103-A-G

46057051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75514050-T-C

46057095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75514008-A-G

46057400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75513699-G-A

http://identifiers.org/hco/13/GRCh38#46057712-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#75512966-A-C

46057855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75512853-A-G

46058010-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75512748-C-G

http://identifiers.org/hco/13/GRCh38#46058041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#75512717-C-A

http://identifiers.org/hco/13/GRCh38#46058170-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#75512591-A-C

46058369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75512392-G-T

46058500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75512273-G-A

46058500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75512273-G-T

46063098-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: -T-A

46063959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75510945-C-T

46063960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75510944-A-G

http://identifiers.org/hco/13/GRCh38#46064512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#75510148-C-A

46064512-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75510148-C-G

http://identifiers.org/hco/13/GRCh38#46064517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#75510142-C-A

46064517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75510142-C-T

46064521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75510138-T-C

46064521-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75510138-T-G

http://identifiers.org/hco/13/GRCh38#46064538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#75510125-C-A

46064711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75509969-A-G

46064711-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75509969-A-T

46064734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75509946-A-G

46065079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75509172-G-T

46067128-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75508407-G-C

46067166-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75508358-T-A

46067166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75508358-T-C

46067224-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75508299-T-G

46067314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75508230-C-T

46067323-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75508221-T-A

46067323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75508221-T-C

46067364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75508180-C-T

46067365-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75508179-A-T

46067413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75508131-G-A

46067413-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75508131-G-C

46067413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75508131-G-T

http://identifiers.org/hco/13/GRCh38#46067523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#75508015-C-A

46067523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75508015-C-T

http://identifiers.org/hco/13/GRCh38#46067540-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#75507998-A-C

46067540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75507998-A-G

46067551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75507987-T-C

46067551-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75507987-T-G

http://identifiers.org/hco/13/GRCh38#46067560-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#75507978-A-C

46067560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75507978-A-G

46067560-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75507978-A-T

46067561-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75507977-G-C

46067561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75507977-G-T

46067767-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75507591-T-A

46068130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75507029-A-G

46068250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75506938-A-G

http://identifiers.org/hco/13/GRCh38#46073393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#75506010-C-A

46073412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75505963-T-C

46073423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75505952-A-G

46073436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75505939-T-C

46073510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 75505874-A-G

46073519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75505865-A-G

46073592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75505785-T-C

http://identifiers.org/hco/13/GRCh38#46073596-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#75505780-A-C

46073783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75505676-T-C

46073818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75505643-A-G

46073818-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75505643-A-T

46073827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75505634-T-C

46073850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75505609-G-A

46073850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75505609-G-T

46073852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75505607-T-C

46073858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75505601-A-G

46074138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75505357-G-A

46074167-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75505334-C-G

46074320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75505206-G-A

46074451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75505084-T-C

46075177-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75504451-A-T

46075224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75504403-A-G

46075420-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75504174-T-A

46075532-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75504062-A-T

46075541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75504053-G-A

46075541-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75504053-G-C

46075682-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75503909-G-C

46075712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75503879-C-T

46075771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75503835-A-G

46075852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75503756-A-G

46075915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75503677-G-A

46076089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75503348-G-A

46078680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75503024-C-T

46078738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75502958-A-G

46078740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75502956-G-A

46078740-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75502956-G-C

46078740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75502956-G-T

http://identifiers.org/hco/13/GRCh38#46078756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#75502940-C-A

46078756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75502940-C-T

46078768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75502928-G-A

46078826-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75502877-C-G

46078875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75502828-A-G

46078921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75502782-A-G

46078961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75502743-A-G

46079008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75502685-G-T

http://identifiers.org/hco/13/GRCh38#46079047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#75502649-C-A

46079065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75502637-A-G

46079109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75502593-G-A

46079522-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75500702-G-C

46079582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75500683-T-C

46079609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75500655-G-T

46079785-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75500514-T-G

46079848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75500484-G-A

http://identifiers.org/hco/13/GRCh38#46079967-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#75500371-A-C

46080080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75500279-G-A

46080385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75500141-A-G

46080412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75500114-G-A

46080603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75499974-T-C

46080605-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75499972-T-G

46080662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75499916-C-T

46081082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75499502-C-T

46081140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75499450-C-T

46081502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75499102-A-G

http://identifiers.org/hco/13/GRCh38#46081515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#75499089-C-A

46082094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75498578-G-A

46082260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75498399-A-G

http://identifiers.org/hco/13/GRCh38#46082317-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#75498342-A-C

46082317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75498342-A-G

46082365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75498295-T-C

http://identifiers.org/hco/13/GRCh38#46082374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#75498284-C-A

46082374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75498284-C-T

46082396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75498262-G-A

46082396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75498262-G-T

46082397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75498261-G-A

46082397-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75498261-G-C

http://identifiers.org/hco/13/GRCh38#46082425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#75498233-C-A

46082425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75498233-C-T

46082466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75498192-T-C

46082516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75498142-T-C

46082523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75498135-A-G

http://identifiers.org/hco/13/GRCh38#46082586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#75498074-C-A

46082620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75498040-G-A

46082620-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75498040-G-C

46082620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75498040-G-T

http://identifiers.org/hco/13/GRCh38#46082624-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#75498036-A-C

46082624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75498036-A-G

46082635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75498025-A-G

46082698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75497984-C-T

46082715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75497966-G-A

46082921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75497401-G-A

46082993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75497345-C-T

46083000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75497338-A-G

46083013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75497325-A-G

46083046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75497289-A-G

46083409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75496774-C-T

46083472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75496723-G-A

46083500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75496697-C-T

46083566-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75496634-T-A

46083906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75495439-G-A

http://identifiers.org/hco/13/GRCh38#46084108-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#75495254-C-A

46084108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75495254-C-T

46084117-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75495245-T-G

46084124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75495238-A-G

46084386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75494973-G-A

46084434-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75494922-A-T

http://identifiers.org/hco/13/GRCh38#46084474-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#75494884-C-A

http://identifiers.org/hco/13/GRCh38#46084477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#75494882-C-A

http://identifiers.org/hco/13/GRCh38#46084481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#75494878-C-A

46084481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75494878-C-T

46084687-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75494708-T-G

46087332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75493815-G-A

46087388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75493760-G-A

46087487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75493668-T-C

46087610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75493562-G-A

46087910-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75493337-A-T

46088195-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75491893-T-G

46088581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75491436-A-G

46088660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75491367-A-G

46088701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75491314-T-C

46088793-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75491223-A-T

46089075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75490846-C-T

46089147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75490584-C-T

46089160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75490500-C-T

46089214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75490454-G-A

http://identifiers.org/hco/13/GRCh38#46089627-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#75490113-C-A

46089772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75489991-G-A

46089772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75489991-G-T

46089777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75489986-A-G

46089900-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75489875-A-T

46090310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75489397-G-A

46091687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75489156-T-C

http://identifiers.org/hco/13/GRCh38#46091747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#75489093-C-A

46091747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75489093-C-T

46092569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75488459-T-C

46093486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75486663-G-A

46093521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75486639-T-C

46093532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75486631-T-C

46093694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75486469-A-G

http://identifiers.org/hco/13/GRCh38#46102244-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#75482277-A-C

46102270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75482251-G-A

46102388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75482144-G-T

46102454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75482068-A-G

46102571-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75481955-T-A

46102634-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75481901-A-T

46102793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75481770-G-A

46102950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75481616-T-C

46103061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75481511-G-A

46103156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75481416-A-G

46103598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75481161-G-A

http://identifiers.org/hco/13/GRCh38#46103790-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#75480915-A-C

46103790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75480915-A-G

46103960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75480756-C-T

46104063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75480681-T-C

46104134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75480608-G-A

46104258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75480502-A-G

46104276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75480486-A-G

46104394-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75480373-G-C

46104502-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75480245-T-G

46104584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75480166-C-T

46104798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75479988-G-T

46104866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75479927-G-T

http://identifiers.org/hco/13/GRCh38#46104961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#75479838-C-A

46105126-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75479682-C-G

46105126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75479682-C-T

http://identifiers.org/hco/13/GRCh38#46105127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#75479681-C-A

46105240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75479549-C-T

46105872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75477914-C-T

46106408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75477748-A-G

46106444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75477713-C-T

http://identifiers.org/hco/13/GRCh38#46120294-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75474209-A-C

46120294-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75474209-A-T

46120382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75474134-G-A

46120382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75474134-G-T

46120446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75474066-A-G

46120611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75473903-G-T

46120642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75473872-G-T

46120700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75473806-T-C

http://identifiers.org/hco/13/GRCh38#46120868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75473639-C-A

http://identifiers.org/hco/13/GRCh38#46120964-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75473556-A-C

46120964-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75473556-A-T

46120981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75473539-G-A

46120981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75473539-G-T

http://identifiers.org/hco/13/GRCh38#46121033-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75473504-C-A

46121033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75473504-C-T

46121150-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75473405-T-A

46121150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75473405-T-C

http://identifiers.org/hco/13/GRCh38#46121217-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75473344-A-C

46121217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75473344-A-G

http://identifiers.org/hco/13/GRCh38#46121290-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75473296-A-C

46121439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75473140-C-T

46121446-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75473133-T-A

46123122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75470969-G-A

46123325-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75470778-G-C

46123516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75470616-G-T

46123543-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75470589-T-G

46123564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75470568-T-C

46123568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75470564-A-G

46123620-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75470513-A-T

46123848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75470283-C-T

46123849-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75470282-A-T

46123958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75469842-G-A

46123958-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75469842-G-C

http://identifiers.org/hco/13/GRCh38#46124213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75469599-C-A

http://identifiers.org/hco/13/GRCh38#46124255-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75469549-A-C

46124282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75469519-G-T

46124450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75468921-G-A

46124487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75468876-T-C

46124538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75468828-G-A

46124650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75468715-A-G

46124755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75468624-C-T

46124759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75468620-C-T

46125799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75468360-C-T

46125810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75468349-G-A

http://identifiers.org/hco/13/GRCh38#46125906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75468290-C-A

46126072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75468118-G-T

http://identifiers.org/hco/13/GRCh38#46126105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#75468086-C-A

46126108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75468083-G-T

http://identifiers.org/hco/13/GRCh38#46126155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#75468036-C-A

46126194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75467995-G-T

http://identifiers.org/hco/13/GRCh38#46126447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#75467785-C-A

46126448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75467784-T-C

46126503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75467710-T-C

http://identifiers.org/hco/13/GRCh38#46126511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#75467696-C-A

46126511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75467696-C-T

46126534-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75467673-A-T

46126596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75467611-C-T

46126639-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75467565-T-G

46126723-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75467485-G-T

46126739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75467469-G-A

46126754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75467454-G-T

46126758-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75467450-C-G

46126758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75467450-C-T

http://identifiers.org/hco/13/GRCh38#46126968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#75467410-C-A

46126968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75467410-C-T

46127108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75467273-G-A

46127108-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75467273-G-C

46127108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75467273-G-T

46127116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75467265-G-A

46127116-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75467265-G-C

46127116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75467265-G-T

46127118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75467263-G-T

46127162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75467235-A-G

http://identifiers.org/hco/13/GRCh38#46127250-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#75467142-A-C

46127250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75467142-A-G

46127257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75467135-T-C

46127270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75467122-A-G

http://identifiers.org/hco/13/GRCh38#46127318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#75467060-C-A

46127321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75467057-G-T

http://identifiers.org/hco/13/GRCh38#46127385-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#75466999-A-C

46127385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75466999-A-G

46127385-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75466999-A-T

http://identifiers.org/hco/13/GRCh38#46127410-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#75466974-A-C

http://identifiers.org/hco/13/GRCh38#46127421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#75466952-C-A

46127421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75466952-C-T

46127462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75466911-A-G

46127476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75466905-G-T

46127588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75466779-G-A

46127679-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75466688-G-C

46127679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75466688-G-T

46128665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75466292-C-T

46128667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75466290-C-T

46129102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75465916-G-A

46129110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75465908-G-A

46129163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75465833-A-G

46129180-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75465816-C-G

46129180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75465816-C-T

46129231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75465313-G-A

46129254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75465290-G-A

46129278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75465266-T-C

46129485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75465065-G-T

http://identifiers.org/hco/13/GRCh38#46129516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75465031-C-A

46129555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75464997-C-T

http://identifiers.org/hco/13/GRCh38#46129561-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75464992-A-C

46129772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75464802-A-G

46130607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75464725-G-T

46130618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75464715-G-T

46130698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75464638-G-T

46130724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75464611-G-A

46130724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75464611-G-T

46130728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75464607-A-G

46130752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75464584-A-G

http://identifiers.org/hco/13/GRCh38#46130759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75464577-C-A

46130759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75464577-C-T

46130795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75464548-T-C

46130892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75464451-G-A

46130986-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75464358-T-A

46130986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75464358-T-C

46132090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75463157-C-T

46132095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75463151-C-T

46132164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75463087-C-T

46132304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75462950-G-A

http://identifiers.org/hco/13/GRCh38#46132387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75462886-C-A

46132424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75462857-C-T

46132772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75462560-A-G

46132772-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75462560-A-T

46132852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75462483-G-A

46132932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75462450-C-T

http://identifiers.org/hco/13/GRCh38#46132959-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75462422-A-C

46133101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75462312-A-G

46133919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75461801-T-C

46134020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75461714-G-A

46134020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75461714-G-T

46134037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75461697-T-C

46134112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75461646-G-A

46134113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75461645-A-G

46134143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75461616-G-A

46134340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75461450-G-A

46134340-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75461450-G-T

http://identifiers.org/hco/13/GRCh38#46134347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75461443-C-A

46134349-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75461441-T-A

46134349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75461441-T-C

46134351-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75461439-G-C

46134363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75461427-G-T

http://identifiers.org/hco/13/GRCh38#46134373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75461417-C-A

46134373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75461417-C-T

46135371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75459958-G-A

46135514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75459823-C-T

46135544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75459793-T-C

http://identifiers.org/hco/13/GRCh38#46135966-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75458989-A-C

46136126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75458885-C-T

46136347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75458685-G-A

46136438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75458586-T-C

46136586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75458435-G-A

46136619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75458402-G-T

46136808-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75458210-A-T

http://identifiers.org/hco/13/GRCh38#46137039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75457995-C-A

46137039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75457995-C-T

46137066-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75457967-G-C

46137250-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75457801-A-T

46137763-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75457282-G-C

http://identifiers.org/hco/13/GRCh38#46137959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75457079-C-A

46137983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75457055-C-T

46137991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75457047-A-G

46138044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75456994-T-C

46138096-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75456945-T-G

46138357-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75456671-A-T

46141975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75454223-G-A

46142001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75454199-T-C

46142022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75454178-C-T

http://identifiers.org/hco/13/GRCh38#46142054-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75454144-A-C

46142059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75454140-G-A

46142151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75454044-A-G

46142172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75454023-T-C

46142178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75454017-A-G

46142204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75453991-G-A

46142204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75453991-G-T

46142207-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75453988-T-A

46142207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75453988-T-C

46142216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75453977-A-G

46142260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75453934-C-T

46142451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75453738-T-C

46142474-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75453717-A-T

46142536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75453657-T-C

http://identifiers.org/hco/13/GRCh38#46142549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75453644-C-A

http://identifiers.org/hco/13/GRCh38#46142560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75453633-C-A

http://identifiers.org/hco/13/GRCh38#46142568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75453625-C-A

46142645-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75453605-A-T

http://identifiers.org/hco/13/GRCh38#46142647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75453603-C-A

46142647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75453603-C-T

http://identifiers.org/hco/13/GRCh38#46142659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75453591-C-A

46142767-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75453444-T-A

46142772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75453439-A-G

46142837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75453374-C-T

http://identifiers.org/hco/13/GRCh38#46142861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75453085-C-A

46142993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75452955-A-G

46143028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75452917-C-T

46143072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75452875-T-C

46143091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75452856-T-C

46143151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75452794-T-C

46143197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75452759-G-T

46143208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75452748-G-A

46143208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75452748-G-T

http://identifiers.org/hco/13/GRCh38#46143269-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#75452683-A-C

46143269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75452683-A-G

46143283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 75452668-T-C

http://identifiers.org/hco/13/GRCh38#46143473-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#75452478-C-A

46143473-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75452478-C-G

46143556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75452405-A-G

46143606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75452364-C-T

46143616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75452353-C-T

46144140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75452278-A-G

46144167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75452255-G-A

46144280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75452149-C-T

46144282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75452147-A-G

http://identifiers.org/hco/13/GRCh38#46144295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75452138-C-A

46144419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75452025-A-G

46144448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75451995-A-G

46144460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75451983-C-T

46144469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75451974-A-G

http://identifiers.org/hco/13/GRCh38#46144487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#75451956-C-A

46144496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75451947-A-G

46144511-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75451932-C-G

46144511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75451932-C-T

46144547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75451898-T-C

46144662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75451806-G-A

46144662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75451806-G-T

46144867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75451674-A-G

46144891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75451641-G-T

46144985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75451547-A-G

46145005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75451527-G-T

46145023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75451512-A-G

46145023-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75451512-A-T

46145035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75451500-C-T

46145037-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75451498-T-A

46145359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75451163-G-A

46145474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75451043-A-G

46145523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75450992-G-A

46145949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75450867-G-A

46145951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75450865-G-A

46146184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75450669-G-A

46146187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75450666-G-A

46146191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75450662-G-T

46146419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75450455-T-C

46146423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75450451-C-T

46146544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75450321-G-A

http://identifiers.org/hco/13/GRCh38#46146783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75450095-C-A

46146804-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75450073-G-C

46146804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75450073-G-T

46146830-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75450047-T-A

46146830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75450047-T-C

46146844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75450032-G-T

46147138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75449735-A-G

46147148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75449727-T-C

46147149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75449726-G-A

46147149-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75449726-G-C

46147209-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75449662-T-A

46147209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75449662-T-C

46147249-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75449622-T-A

46147585-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75449299-A-T

46147870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75449026-G-A

46147957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75448952-C-T

46147959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75448950-T-C

http://identifiers.org/hco/13/GRCh38#46148017-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75448891-A-C

46148033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75448874-G-T

46148195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75448111-T-C

46148260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75448054-G-A

46148260-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75448054-G-T

http://identifiers.org/hco/13/GRCh38#46148281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75448042-C-A

46148281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75448042-C-T

http://identifiers.org/hco/13/GRCh38#46148401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#75447923-C-A

46148485-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75447838-C-G

46148485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75447838-C-T

46148559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75447765-A-G

http://identifiers.org/hco/13/GRCh38#46148689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#75447633-C-A

46148689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75447633-C-T

46148824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75447505-A-G

46148923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75447414-G-A

46148923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75447414-G-T

46149589-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75446805-G-C

46149589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75446805-G-T

46149658-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75446779-G-C

46149735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75446733-A-G

46149968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75446525-A-G

46150204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75446290-G-A

46150399-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75446120-T-A

46150399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75446120-T-C

46150446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75446088-G-A

46150946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75445990-G-A

46150946-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75445990-G-C

46150967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75445969-T-C

46150967-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75445969-T-G

46150976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75445960-G-T

46151045-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75445891-A-T

http://identifiers.org/hco/13/GRCh38#46151103-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75445832-A-C

46151112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75445823-G-T

46151150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75445786-A-G

http://identifiers.org/hco/13/GRCh38#46151230-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75445709-A-C

46151456-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75445480-T-G

46151562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75445374-C-T

46151888-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75444818-C-G

46152104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75444299-G-T

46152517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75443972-G-A

46152522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75443967-T-C

http://identifiers.org/hco/13/GRCh38#46152663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75443836-C-A

http://identifiers.org/hco/13/GRCh38#46152724-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75443778-A-C

46152730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75443772-T-C

46152744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75443758-G-A

46152744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75443758-G-T

46152750-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75443752-T-G

46153015-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75443485-A-T

46153016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75443484-G-A

46153016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75443484-G-T

46153023-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75443477-T-A

46153023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75443477-T-C

46153035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75443465-G-T

46153041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75443459-G-A

46153041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75443459-G-T

46153059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75443441-T-C

46153079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75443421-A-G

46153111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75443392-G-A

46153111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75443392-G-T

46153123-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75443380-T-A

http://identifiers.org/hco/13/GRCh38#46153147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75443357-C-A

46153147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75443357-C-T

http://identifiers.org/hco/13/GRCh38#46153189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75443315-C-A

46153200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75443308-G-A

46153200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75443308-G-T

46153271-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75443237-T-A

46153271-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75443237-T-G

46153313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75443214-G-A

46153313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75443214-G-T

46153334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75443193-G-T

46153776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75443059-G-A

46153776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75443059-G-T

46153803-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75443029-A-T

http://identifiers.org/hco/13/GRCh38#46153866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75442973-C-A

46154002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75442844-G-A

http://identifiers.org/hco/13/GRCh38#46154453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75442419-C-A

46154528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75442345-T-C

46154714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75442162-G-A

46154714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75442162-G-T

46154763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75442126-G-A

46154763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75442126-G-T

46154839-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75442050-A-T

http://identifiers.org/hco/13/GRCh38#46154866-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#75442023-A-C

http://identifiers.org/hco/13/GRCh38#46155027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75441865-C-A

46155027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75441865-C-T

46155040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75441851-C-T

46155104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75441802-G-A

46155104-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75441802-G-C

46155975-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75441477-A-T

http://identifiers.org/hco/13/GRCh38#46156342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75440298-C-A

46156342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75440298-C-T

46156357-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75440284-G-T

46156477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75440167-T-C

46156492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75440152-A-G

46156498-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75440146-A-T

46157219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75439861-T-C

46157589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75439496-A-G

46157647-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75439446-T-A

46157647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75439446-T-C

46157666-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75439427-G-C

46157687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75439406-C-T

46158168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75438347-T-C

46158291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75438236-C-T

46158325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75438201-T-C

46158389-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75438137-T-A

46158389-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75438137-T-G

http://identifiers.org/hco/13/GRCh38#46158447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75438083-C-A

46158447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75438083-C-T

http://identifiers.org/hco/13/GRCh38#46158479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75438051-C-A

http://identifiers.org/hco/13/GRCh38#46158486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75438044-C-A

46158486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75438044-C-T

46158545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 75437924-A-G

46158545-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 75437924-A-T

46158585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 75437884-C-T

46158586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 75437883-T-C

46158586-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 75437883-T-G

46158665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75437035-A-G

46158665-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75437035-A-T

46158724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75436977-G-A

46158742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75436959-G-A

46158746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75436955-T-C

46158798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75436910-G-A

46159030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75436677-G-A

46159066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75436642-G-A

46159066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75436642-G-T

46159067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75436641-G-A

46159067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75436641-G-T

http://identifiers.org/hco/13/GRCh38#46159082-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75436627-A-C

46159082-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75436627-A-T

46159107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75436608-G-T

46159127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75436589-T-C

46159157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75436559-G-A

46159157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75436559-G-T

http://identifiers.org/hco/13/GRCh38#46159159-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75436557-A-C

http://identifiers.org/hco/13/GRCh38#46159598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: non_coding_transcript_exon_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75435602-C-A

46159646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 75435554-A-G

46159700-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75435505-G-C

46159700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75435505-G-T

46159715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75435491-C-T

http://identifiers.org/hco/13/GRCh38#46159744-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75435473-A-C

46159796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75435417-C-T

46159924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75435322-A-G

46159932-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75435314-A-T

46160088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75435150-C-T

46160468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75434855-A-G

46160874-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75434517-T-A

46160916-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75434471-C-G

46160945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75434442-T-C

http://identifiers.org/hco/13/GRCh38#46160982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75434405-C-A

46161057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75434319-A-G

46161261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39898
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75434079-C-T