55428096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 76357873-C-T

55428198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 76357998-C-T

55428275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 76358056-T-C

http://identifiers.org/hco/4/GRCh38#55428325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#76358105-C-A

55428564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 76358309-G-A

http://identifiers.org/hco/4/GRCh38#55428970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#76358703-C-A

55428970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 76358703-C-T

http://identifiers.org/hco/4/GRCh38#55429472-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#76359200-A-C

55429860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 76359521-A-G

http://identifiers.org/hco/4/GRCh38#55429894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#76359553-C-A

55429968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 76359633-G-T

55430366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 76359980-A-G

55430366-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 76359980-A-T

55431340-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 76360933-G-T

55431923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 76361483-T-C

55432365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 76361916-G-A

55432365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 76361916-G-T

55432498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76362054-T-C

http://identifiers.org/hco/4/GRCh38#55432668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#76362207-C-A

http://identifiers.org/hco/4/GRCh38#55432718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#76362253-C-A

55432718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76362253-C-T

http://identifiers.org/hco/4/GRCh38#55433437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#76362741-C-A

55433478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76362772-G-T

55433498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76362792-T-C

http://identifiers.org/hco/4/GRCh38#55433580-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#76362860-A-C

55434070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76363274-T-C

55434319-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76363499-T-A

55434608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76363781-T-C

55434919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76364083-G-A

55434919-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76364083-G-C

55434919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76364083-G-T

http://identifiers.org/hco/4/GRCh38#55434930-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#76364094-A-C

http://identifiers.org/hco/4/GRCh38#55435220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#76364365-C-A

55435258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76364403-G-A

55435258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76364403-G-T

http://identifiers.org/hco/4/GRCh38#55435314-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#76364455-A-C

http://identifiers.org/hco/4/GRCh38#55435379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#76364512-C-A

55435383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76364516-C-T

55435387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76364520-C-T

55435388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76364521-T-C

55435577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 76364708-A-G

55435678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76364798-T-C

55435740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76364844-T-C

55436470-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76372947-T-G

55436860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76373300-A-G

55436860-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76373300-A-T

55437575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76374013-G-A

55437575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76374013-G-T

55437822-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76374246-T-G

55438063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76374566-T-C

55438145-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76374648-T-A

http://identifiers.org/hco/4/GRCh38#55438165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#76374668-C-A

55438165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76374668-C-T

55438196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76374699-T-C

http://identifiers.org/hco/4/GRCh38#55438203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#76374705-C-A

55438203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76374705-C-T

55438601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76375122-G-A

55438657-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76375175-A-T

http://identifiers.org/hco/4/GRCh38#55442545-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#76377318-A-C

55442694-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76377456-T-G

http://identifiers.org/hco/4/GRCh38#55442714-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#76377478-A-C

55442735-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76377492-G-C

55442735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76377492-G-T

55443770-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76378083-T-A

55443770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76378083-T-C

55443774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 76378087-G-A

55443936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76378318-T-C

55444008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76378598-G-T

55444120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76378764-G-A

55444147-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76378797-T-G

55444386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76379002-C-T

http://identifiers.org/hco/4/GRCh38#55444441-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#76379048-A-C

55444805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76379415-A-G

55446445-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76381372-C-G

55447619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76382533-T-C

http://identifiers.org/hco/4/GRCh38#55447945-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#76382845-A-C

55448042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76382919-G-A

http://identifiers.org/hco/4/GRCh38#55448181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#76383161-C-A

55448716-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76383555-A-T

http://identifiers.org/hco/4/GRCh38#55448927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#76383762-C-A

55449170-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76383975-T-A

55449411-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 76384144-T-G

55449624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, undefined
orthologous variants: 76384342-T-C

55449649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, undefined
orthologous variants: 76384367-G-A

http://identifiers.org/hco/4/GRCh38#55449986-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#76384764-A-C

55450276-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, undefined
orthologous variants: 76385054-C-G

55450276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, undefined
orthologous variants: 76385054-C-T

http://identifiers.org/hco/4/GRCh38#55452881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76388605-C-A

http://identifiers.org/hco/4/GRCh38#55452892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76388616-C-A

55452892-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76388616-C-G

55452892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76388616-C-T

http://identifiers.org/hco/4/GRCh38#55453050-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76388714-A-C

55453216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76388879-G-T

http://identifiers.org/hco/4/GRCh38#55453228-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76388891-C-A

55453228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76388891-C-T

55453236-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76388906-C-G

55453236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76388906-C-T

http://identifiers.org/hco/4/GRCh38#55453340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76389399-C-A

55453340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76389399-C-T

55453382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76389442-A-G

http://identifiers.org/hco/4/GRCh38#55453588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76389643-C-A

55453588-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron variant
orthologous variants: 76389643-C-G

55453787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 76389827-C-T

http://identifiers.org/hco/4/GRCh38#55453888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76389960-C-A

55453888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76389960-C-T

55454024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76390095-A-G

55454240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76390314-G-A

http://identifiers.org/hco/4/GRCh38#55455748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76390520-C-A

55455748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76390520-C-T

55456055-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76390781-T-A

55456148-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76390868-T-A

http://identifiers.org/hco/4/GRCh38#55456340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76391055-C-A

55457414-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76391779-G-C

55457695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76392066-C-T

55458672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76392829-C-T

http://identifiers.org/hco/4/GRCh38#55458803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76392924-C-A

55458803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76392924-C-T

http://identifiers.org/hco/4/GRCh38#55458811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76392933-C-A

55458811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76392933-C-T

55458821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76392943-T-C

55458821-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76392943-T-G

55458898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 76393049-G-A

55458898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76393049-G-T

55458968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76393119-C-T

http://identifiers.org/hco/4/GRCh38#55461849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76394192-C-A

55461945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76394291-G-A

55462125-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76394450-T-G

55463838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76396342-T-C

55464353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76396823-A-G

55464476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76396925-C-T

http://identifiers.org/hco/4/GRCh38#55464481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76396930-C-A

55464527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76396982-G-A

55464622-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76397021-T-G

55464768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76397130-G-A

55465984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76398721-C-T

55466572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76398906-T-C

55466673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76398999-A-G

55466879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76399235-G-A

55468240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76401118-G-A

55468245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76401123-C-T

http://identifiers.org/hco/4/GRCh38#55470609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76402116-C-A

55470898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76402394-A-G

55471084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76402578-A-G

55471260-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76402686-T-G

55472357-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76403295-C-G

55472832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76403895-G-T

55472841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76403904-G-T

55475923-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76410482-T-G

55475924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76410483-G-A

55475924-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76410483-G-C

55476160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76410711-T-C

55476162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76410713-G-A

http://identifiers.org/hco/4/GRCh38#55476164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76410715-C-A

55476164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76410715-C-T

55476425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76410979-C-T

55476555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76411052-T-C

55477153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76412015-T-C

55477232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76412092-T-C

55477825-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76412655-T-A

55477825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76412655-T-C

55478630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76413493-G-A

55479616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76414180-A-G

http://identifiers.org/hco/4/GRCh38#55479721-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76414285-A-C

55479776-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76414336-T-A

http://identifiers.org/hco/4/GRCh38#55479777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76414337-C-A

55479777-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76414337-C-G

55479783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76414343-T-C

55479790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76414347-T-C

55480014-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76414562-G-C

55483121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76414981-T-C

55483354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76415205-C-T

55483478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76415302-A-G

http://identifiers.org/hco/4/GRCh38#55483642-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76415440-A-C

55484041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76415804-G-A

55484051-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76415811-G-C

55484387-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76416113-A-T

55484571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76416294-G-A

http://identifiers.org/hco/4/GRCh38#55484700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76416396-C-A

55485288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76416651-C-T

55489292-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76421723-G-C

55489357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76421795-G-A

55489357-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76421795-G-T

http://identifiers.org/hco/4/GRCh38#55493331-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76429723-A-C

55498101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76430445-T-C

http://identifiers.org/hco/4/GRCh38#55498326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76431400-C-A

55498535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76431678-C-T

55498763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76431988-G-A

55541113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76448348-C-T

http://identifiers.org/hco/4/GRCh38#55541716-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76448938-C-A

55541786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76448999-G-A

http://identifiers.org/hco/4/GRCh38#55543218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76449233-C-A

55543314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76449340-T-C

55543760-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76449821-G-C

55543982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76450039-C-T

55544301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76450454-C-T

55544345-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76450493-G-C

55544436-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76450568-A-T

55544570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76450666-C-T

55545073-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76451050-T-G

http://identifiers.org/hco/4/GRCh38#55545570-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76451406-A-C

http://identifiers.org/hco/4/GRCh38#55545631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76451461-C-A

55545715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76451543-T-C

55545792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76451605-A-G

55545920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 76451650-G-A

55545929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 76451659-A-G

55545960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 76451690-G-T

55545978-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 76451708-C-G

55546049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 76451776-C-T

http://identifiers.org/hco/4/GRCh38#55546317-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76452040-A-C

55546333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76452058-G-T

http://identifiers.org/hco/4/GRCh38#55546413-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#76452142-A-C

55546417-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76452146-T-A

55546417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76452146-T-C

http://identifiers.org/hco/4/GRCh38#55546432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#76452162-C-A

55546432-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 76452162-C-G

55546432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 76452162-C-T

http://identifiers.org/hco/4/GRCh38#55546450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#76452190-C-A

55546450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 76452190-C-T

http://identifiers.org/hco/4/GRCh38#55546594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#76452320-C-A

55546594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 76452320-C-T

55546620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 76452347-G-A

55546620-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 76452347-G-C

55546620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2082
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 76452347-G-T