46053420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75521017-A-G

46053481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75520953-T-C

46053543-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75520918-T-A

46053543-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75520918-T-G

46053604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75520869-A-G

46053656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 75520811-G-A

46055195-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75517449-A-T

46055325-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75517355-C-G

46055379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75517315-A-G

46055932-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75515479-A-T

46055934-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75515477-T-A

46055963-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75515448-T-A

46056370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75515063-A-G

46056557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75514903-T-C

46056670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75514322-T-C

46056997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75514103-A-G

46057051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75514050-T-C

46057095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75514008-A-G

46057400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_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: 2300
most severe consequence: NMD_transcript_variant, intron_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: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75512853-A-G

46058010-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_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: 2300
most severe consequence: NMD_transcript_variant, intron_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: 2300
most severe consequence: NMD_transcript_variant, intron_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: 2300
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 75512392-G-T

46058500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75512273-G-A

46058500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75512273-G-T

46063098-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: -T-A

46063959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75510945-C-T

46063960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_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: 2300
most severe consequence: NMD_transcript_variant, intron_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: 2300
most severe consequence: NMD_transcript_variant, intron_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: 2300
most severe consequence: NMD_transcript_variant, intron_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: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75510142-C-T

46064521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75510138-T-C

46064521-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_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: 2300
most severe consequence: NMD_transcript_variant, intron_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: 2300
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 75509969-A-G

46064711-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 75509969-A-T

46064734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 75509946-A-G

46065079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75509172-G-T

46067128-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75508407-G-C

46067166-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75508358-T-A

46067166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75508358-T-C

46067224-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75508299-T-G

46067314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, stop_gained, undefined
orthologous variants: 75508230-C-T

46067323-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 75508221-T-A

46067323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 75508221-T-C

46067364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 75508180-C-T

46067365-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 75508179-A-T

46067413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 75508131-G-A

46067413-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 75508131-G-C

46067413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, missense_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: 2300
most severe consequence: NMD_transcript_variant, intron_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: 2300
most severe consequence: NMD_transcript_variant, intron_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: 2300
most severe consequence: NMD_transcript_variant, intron_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: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75507998-A-G

46067551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75507987-T-C

46067551-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_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: 2300
most severe consequence: NMD_transcript_variant, intron_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: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75507978-A-G

46067560-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75507978-A-T

46067561-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75507977-G-C

46067561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75507977-G-T

46067767-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75507591-T-A

46068130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75507029-A-G

46068250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_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: 2300
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_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: 2300
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75505963-T-C

46073423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75505952-A-G

46073436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75505939-T-C

46073510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_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: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75505865-A-G

46073592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_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: 2300
most severe consequence: NMD_transcript_variant, intron_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: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75505676-T-C

46073818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75505643-A-G

46073818-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75505643-A-T

46073827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75505634-T-C

46073850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75505609-G-A

46073850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75505609-G-T

46073852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75505607-T-C

46073858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75505601-A-G

46074138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75505357-G-A

46074167-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75505334-C-G

46074320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75505206-G-A

46074451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75505084-T-C

46075177-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75504451-A-T

46075224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75504403-A-G

46075420-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75504174-T-A

46075532-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75504062-A-T

46075541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75504053-G-A

46075541-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75504053-G-C

46075682-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75503909-G-C

46075712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75503879-C-T

46075771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75503835-A-G

46075852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75503756-A-G

46075915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75503677-G-A

46076089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75503348-G-A

46078680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75503024-C-T

46078738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75502958-A-G

46078740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75502956-G-A

46078740-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75502956-G-C

46078740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_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: 2300
most severe consequence: NMD_transcript_variant, intron_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: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75502940-C-T

46078768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75502928-G-A

46078826-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 75502877-C-G

46078875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 75502828-A-G

46078921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75502782-A-G

46078961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75502743-A-G

46079008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_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: 2300
most severe consequence: NMD_transcript_variant, intron_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: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75502637-A-G

46079109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75502593-G-A

46079522-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75500702-G-C

46079582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75500683-T-C

46079609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75500655-G-T

46079785-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75500514-T-G

46079848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_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: 2300
most severe consequence: NMD_transcript_variant, intron_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: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75500279-G-A

46080385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75500141-A-G

46080412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75500114-G-A

46080603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75499974-T-C

46080605-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75499972-T-G

46080662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75499916-C-T

46081082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75499502-C-T

46081140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75499450-C-T

46081502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_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: 2300
most severe consequence: NMD_transcript_variant, intron_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: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75498578-G-A

46082260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_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: 2300
most severe consequence: NMD_transcript_variant, intron_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: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75498342-A-G

46082365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_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: 2300
most severe consequence: NMD_transcript_variant, intron_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: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75498284-C-T

46082396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75498262-G-A

46082396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75498262-G-T

46082397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75498261-G-A

46082397-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_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: 2300
most severe consequence: NMD_transcript_variant, intron_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: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75498233-C-T

46082466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 75498192-T-C

46082516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 75498142-T-C

46082523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, missense_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: 2300
most severe consequence: NMD_transcript_variant, intron_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: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75498040-G-A

46082620-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75498040-G-C

46082620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_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: 2300
most severe consequence: NMD_transcript_variant, intron_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: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75498036-A-G

46082635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75498025-A-G

46082698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75497984-C-T

46082715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75497966-G-A

46082921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75497401-G-A

46082993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75497345-C-T

46083000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75497338-A-G

46083013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75497325-A-G

46083046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75497289-A-G

46083409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75496774-C-T

46083472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75496723-G-A

46083500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75496697-C-T

46083566-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75496634-T-A

46083906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_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: 2300
most severe consequence: NMD_transcript_variant, intron_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: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75495254-C-T

46084117-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75495245-T-G

46084124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75495238-A-G

46084386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75494973-G-A

46084434-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_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: 2300
most severe consequence: NMD_transcript_variant, intron_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: 2300
most severe consequence: NMD_transcript_variant, intron_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: 2300
most severe consequence: NMD_transcript_variant, intron_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: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75494878-C-T

46084687-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75494708-T-G

46087332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75493815-G-A

46087388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75493760-G-A

46087487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75493668-T-C

46087610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75493562-G-A

46087910-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75493337-A-T

46088195-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75491893-T-G

46088581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75491436-A-G

46088660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75491367-A-G

46088701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75491314-T-C

46088793-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75491223-A-T

46089075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75490846-C-T

46089147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75490584-C-T

46089160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75490500-C-T

46089214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_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: 2300
most severe consequence: NMD_transcript_variant, intron_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: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75489991-G-A

46089772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75489991-G-T

46089777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75489986-A-G

46089900-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75489875-A-T

46090310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75489397-G-A

46091687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_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: 2300
most severe consequence: NMD_transcript_variant, intron_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: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75489093-C-T

46092569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75488459-T-C

46093486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75486663-G-A

46093521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75486639-T-C

46093532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75486631-T-C

46093694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_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: 2300
most severe consequence: NMD_transcript_variant, intron_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: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75482251-G-A

46102388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75482144-G-T

46102454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75482068-A-G

46102571-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75481955-T-A

46102634-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75481901-A-T

46102793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75481770-G-A

46102950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75481616-T-C

46103061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75481511-G-A

46103156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75481416-A-G

46103598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_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: 2300
most severe consequence: NMD_transcript_variant, intron_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: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75480915-A-G

46103960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75480756-C-T

46104063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75480681-T-C

46104134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75480608-G-A

46104258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75480502-A-G

46104276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75480486-A-G

46104394-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75480373-G-C

46104502-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75480245-T-G

46104584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75480166-C-T

46104798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75479988-G-T

46104866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2300
most severe consequence: NMD_transcript_variant, intron_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: 2300
most severe consequence: NMD_transcript_variant, intron_variant, stop_gained, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#75479838-C-A