http://identifiers.org/hco/5/GRCh38#55738068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112788841-C-A

55738068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112788841-C-T

http://identifiers.org/hco/5/GRCh38#55738093-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112788816-C-A

55738093-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112788816-C-G

55738093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112788816-C-T

55738121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112788783-A-G

http://identifiers.org/hco/5/GRCh38#55738128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112788781-C-A

55738128-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112788781-C-G

55738128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112788781-C-T

55738220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112788662-G-T

55738229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112788653-C-T

http://identifiers.org/hco/5/GRCh38#55738250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112788617-C-A

55738250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112788617-C-T

55738268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112788606-G-T

55738288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112788580-G-T

http://identifiers.org/hco/5/GRCh38#55738398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112788490-C-A

55738398-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112788490-C-G

55738398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112788490-C-T

http://identifiers.org/hco/5/GRCh38#55738445-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112788480-A-C

55738445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112788480-A-G

55738445-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112788480-A-T

http://identifiers.org/hco/5/GRCh38#55738449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112788476-C-A

55738449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112788476-C-T

55738470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112788455-G-A

55738470-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112788455-G-C

55738470-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112788455-G-T

55738506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112788446-C-T

55738625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112788335-A-G

55738693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112788279-A-G

http://identifiers.org/hco/5/GRCh38#55738872-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112788104-A-C

http://identifiers.org/hco/5/GRCh38#55738927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112788012-C-A

55738927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112788012-C-T

55738943-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 112787956-T-A

55738943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 112787956-T-C

55738943-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 112787956-T-G

55738944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 112787955-G-A

55738944-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 112787955-G-C

55738944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 112787955-G-T

55739012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112787884-T-C

http://identifiers.org/hco/5/GRCh38#55739140-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112787761-A-C

http://identifiers.org/hco/5/GRCh38#55739698-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112787325-A-C

55739806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112787229-A-G

55740875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112786917-A-G

55741037-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112786755-G-C

55741080-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112786713-T-G

55741117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112786676-T-C

55741941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112786040-T-C

http://identifiers.org/hco/5/GRCh38#55742015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112785988-C-A

55742015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112785988-C-T

55742193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 112785836-A-G

55742194-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 112785835-T-G

55742195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 112785834-T-C

55742701-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112785404-A-T

55742839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112785261-T-C

55743033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112785097-G-A

55743033-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112785097-G-C

55743141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112785001-G-A

55743167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112784976-C-T

55744400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112783529-T-C

55744525-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112783255-T-G

55744601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112783176-T-C

55744616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112783161-A-G

55744639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112783138-G-A

55744850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112782944-A-G

55745345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112782159-T-C

55746301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112780996-A-G

55746301-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112780996-A-T

55746664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112780654-A-G

http://identifiers.org/hco/5/GRCh38#55746802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112780536-C-A

55746802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112780536-C-T

55747729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112779769-C-T

55748375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112779181-T-C

55748813-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112778551-T-G

55748859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112778504-G-A

55748871-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112778487-T-G

55748902-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112778456-G-C

55748953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112778406-C-T

55748974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112778386-A-G

55760099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112777862-T-C

http://identifiers.org/hco/5/GRCh38#55760184-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112777775-A-C

55760184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112777775-A-G

55760227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112777732-A-G

55760282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112777677-G-A

55760282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112777677-G-T

55760299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112777663-T-C

55760411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112777559-G-A

55760413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112777552-T-C

55760445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112777520-T-C

55761022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112775461-T-C

55761318-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112775012-A-T

55762270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112774188-G-T

http://identifiers.org/hco/5/GRCh38#55762392-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112773818-A-C

55762392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112773818-A-G

55762838-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112772889-T-A

55763142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112772603-T-C

55763837-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112770869-T-A

55763857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112770850-A-G

55763901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112770807-G-T

55764107-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112770370-T-A

55764107-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112770370-T-G

55764168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112770319-T-C

55764398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112770027-T-C

55765324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112768528-G-A

55765456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112768427-G-T

55765491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112768387-C-T

55765577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112768311-A-G

55766930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112765998-A-G

http://identifiers.org/hco/5/GRCh38#55766959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112765969-C-A

55766959-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 112765969-C-G

55766959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 112765969-C-T

55767483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112765758-T-C

55767502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112765730-A-G

55767683-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112765604-G-C

55768040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112765280-A-G

http://identifiers.org/hco/5/GRCh38#55768052-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112765270-A-C

55768052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112765270-A-G

55768094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112765228-G-A

http://identifiers.org/hco/5/GRCh38#55768096-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112765226-A-C

55768096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 112765226-A-G

55770213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112765185-T-C

55770505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112764903-G-A

55770521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112764887-G-A

55770593-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112764818-A-T

http://identifiers.org/hco/5/GRCh38#55770706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112764718-C-A

http://identifiers.org/hco/5/GRCh38#55770757-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112764675-A-C

55779623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112763319-G-A

55780163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112762788-T-C

55780342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112762615-A-G

55780370-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112762587-C-G

55780592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112762379-C-T

55780694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112762247-G-A

55780726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112762218-A-G

55780976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112762024-G-T

55781158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112761865-A-G

55781176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112761849-A-G

55781386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112761646-A-G

55781797-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112761488-T-A

55781798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112761487-A-G

55781801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112761484-A-G

55781802-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112761483-T-A

http://identifiers.org/hco/5/GRCh38#55781834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112761458-C-A

55781834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112761458-C-T

http://identifiers.org/hco/5/GRCh38#55781835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112761457-C-A

55781872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112761427-G-A

55781892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112761395-G-A

55781893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112761394-C-T

55781910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112761378-A-G

55782014-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112761282-T-G

55782085-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112761247-T-G

55782184-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112761156-T-A

55782184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112761156-T-C

55782184-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112761156-T-G

55782246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112761094-G-A

55782246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112761094-G-T

55784596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112760096-A-G

55784686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112760007-G-A

55784785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112759936-G-A

55784832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112759918-G-A

55784885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112759884-C-T

55784970-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112759805-T-G

55785043-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112759731-C-G

55785080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112759694-A-G

55785149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112759627-A-G

http://identifiers.org/hco/5/GRCh38#55785171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112759547-C-A

55785171-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112759547-C-G

55785247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112759427-T-C

55785523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112759064-G-A

55785523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112759064-G-T

55785525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112759062-A-G

55785643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112758917-T-C

http://identifiers.org/hco/5/GRCh38#55785670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112758891-C-A

55785670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112758891-C-T

55785679-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112758882-T-A

http://identifiers.org/hco/5/GRCh38#55785690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112758871-C-A

55785978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112758618-A-G

55786455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112757962-T-C

55786745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112757641-T-C

55786797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112757593-G-T

55788017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112757125-G-A

55788017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112757125-G-T

55788024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112757118-A-G

http://identifiers.org/hco/5/GRCh38#55788151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112757015-C-A

55790523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112750407-G-T

55790525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112750405-T-C

55790619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 112750315-G-A

http://identifiers.org/hco/5/GRCh38#55790744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112750192-C-A

55792564-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112748758-A-T

55792607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112748710-A-G

55792889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112748415-T-C

55793808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112747422-T-C

55794528-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112746915-G-C

55794528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112746915-G-T

55797609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112742129-G-A

55797728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112742062-A-G

55797933-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112741915-C-G

55797942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112741906-G-A

55798012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112741845-T-C

55798022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112741833-A-G

http://identifiers.org/hco/5/GRCh38#55798076-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112741510-A-C

55798334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112741272-A-G

55798334-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112741272-A-T

55798403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112741191-A-G

55798436-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 112741154-G-C

55798450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 112741140-A-G

55798463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 112741127-G-T

55798511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 112741079-G-A

55798609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112740981-A-G

55798906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112740614-A-G

55799965-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112739249-G-T

55813099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112738592-T-C

55813106-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112738585-T-A

55813359-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112738347-T-A

55813359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112738347-T-C

55813512-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112738179-C-G

55813557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112738128-G-A

55813557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112738128-G-T

55815391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 112736185-G-A

55815467-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron variant
orthologous variants: 112736110-T-A

55815467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron variant
orthologous variants: 112736110-T-C

55815583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron variant
orthologous variants: 112736038-A-G

55816206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron variant
orthologous variants: 112735807-G-A

http://identifiers.org/hco/5/GRCh38#55816405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112735613-C-A

55816405-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron variant
orthologous variants: 112735613-C-G

55816405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: intron variant
orthologous variants: 112735613-C-T

55816654-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: 3 prime UTR variant
orthologous variants: 112735361-T-G

55816678-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: 3 prime UTR variant
orthologous variants: 112735337-A-T

http://identifiers.org/hco/5/GRCh38#55816687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#112735325-C-A

55816687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: 3 prime UTR variant
orthologous variants: 112735325-C-T

55816709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18700
most severe consequence: 3 prime UTR variant
orthologous variants: 112735303-A-G