55853655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 76677165-T-C

55853700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 76677215-G-A

55853700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 76677215-G-T

55853769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 76677289-G-A

55853807-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 76677319-C-G

55853807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 76677319-C-T

55853953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant, undefined
orthologous variants: 76677429-G-A

55853953-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant, undefined
orthologous variants: 76677429-G-C

55853996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, undefined
orthologous variants: 76677475-T-C

55853999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, undefined
orthologous variants: 76677478-G-T

55854007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, undefined
orthologous variants: 76677486-A-G

http://identifiers.org/hco/4/GRCh38#55854184-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76677621-A-C

55854184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76677621-A-G

55854184-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76677621-A-T

55854250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76677677-C-T

55854306-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76677730-A-T

55854427-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76677887-G-C

55854522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76677980-A-G

55854542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76678009-A-G

55854765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76678190-G-T

55855015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76678473-C-T

55855023-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76678481-T-G

55855237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76678691-G-A

55858103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76680431-A-G

55858109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76680437-A-G

55858240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76680535-A-G

55858350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 76680638-A-G

55858524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76680786-A-G

http://identifiers.org/hco/4/GRCh38#55858564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76680826-C-A

http://identifiers.org/hco/4/GRCh38#55859212-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76682150-A-C

55859212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76682150-A-G

55859473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76682386-A-G

55859473-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76682386-A-T

55859483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76682396-A-G

55859533-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76682460-G-C

55859925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76682931-A-G

55860235-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76683228-A-T

http://identifiers.org/hco/4/GRCh38#55860270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76683263-C-A

55860270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76683263-C-T

http://identifiers.org/hco/4/GRCh38#55860316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76683304-C-A

55860316-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76683304-C-G

55860368-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76683355-A-T

55860372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76683359-G-A

http://identifiers.org/hco/4/GRCh38#55860460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76683450-C-A

55860460-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 76683450-C-G

55860460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 76683450-C-T

55860554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76683544-C-T

55860649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76683724-G-A

55860649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76683724-G-T

55860662-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76683738-T-G

55860899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76683995-A-G

55860983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76684055-G-A

55861165-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76684185-A-T

http://identifiers.org/hco/4/GRCh38#55861285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76684310-C-A

55863676-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76684977-T-G

55863789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76685081-T-C

55863951-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76685213-A-T

55863967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76685230-A-G

http://identifiers.org/hco/4/GRCh38#55864174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76685495-C-A

55864174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76685495-C-T

55864213-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76685530-T-A

55864213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76685530-T-C

55864337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 76685655-T-C

55864395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76685712-A-G

55864512-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76685834-T-G

55864624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76686156-C-T

55865091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76686483-A-G

55865184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76686569-A-G

55865406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76687237-T-C

55865758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76687564-C-T

55865826-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76687636-T-A

55865885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76687678-G-A

55866136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76687918-A-G

http://identifiers.org/hco/4/GRCh38#55866177-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76687965-A-C

55866755-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76688478-A-T

55866776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76688500-G-A

55866776-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76688500-G-C

55866776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76688500-G-T

55866824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76688548-A-G

55866962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76688683-G-T

55866992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76688713-A-G

55867276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76689001-T-C

55867326-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76689133-C-G

55867401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76689207-G-A

55868306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76689868-T-C

55868487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 76690049-A-G

http://identifiers.org/hco/4/GRCh38#55868535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76690099-C-A

55868535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76690099-C-T

55868569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76690126-G-T

55868571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76690141-G-A

55868574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76690144-G-A

http://identifiers.org/hco/4/GRCh38#55868636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76690204-C-A

http://identifiers.org/hco/4/GRCh38#55868658-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76690224-A-C

55868658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76690224-A-G

http://identifiers.org/hco/4/GRCh38#55868724-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76690613-A-C

55868747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76690642-G-A

55868747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76690642-G-T

55868775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76690670-G-A

http://identifiers.org/hco/4/GRCh38#55868778-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76690673-A-C

http://identifiers.org/hco/4/GRCh38#55868781-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76690676-A-C

55868793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76690691-A-G

55868805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76690701-G-A

55868807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76690703-T-C

http://identifiers.org/hco/4/GRCh38#55868812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76690708-C-A

55868812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76690708-C-T

55868902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76690791-A-G

55868973-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76690852-T-G

55868974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76690853-G-A

55870595-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76691244-T-A

55870608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76691260-A-G

55870608-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76691260-A-T

55870919-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76691543-T-A

http://identifiers.org/hco/4/GRCh38#55871314-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76691931-A-C

55871314-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76691931-A-T

55871377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76691986-A-G

55871377-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76691986-A-T

55871704-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76692704-C-G

55871704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76692704-C-T

55871729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76692729-A-G

55871744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76692744-A-G

55871752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76692751-G-T

55871995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76693247-A-G

55872041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76693297-A-G

55872260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76693488-A-G

55872320-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76693542-G-C

55872545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76693755-A-G

55872843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76694012-T-C

55872843-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76694012-T-G

55872941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76694111-G-A

http://identifiers.org/hco/4/GRCh38#55873200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76694298-C-A

55873200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76694298-C-T

55873201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76694299-G-A

55873352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76694407-A-G

http://identifiers.org/hco/4/GRCh38#55873745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76694749-C-A

55873774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76694780-C-T

55875586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76695708-G-A

55875586-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76695708-G-C

55875695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76695831-A-G

55875697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76695833-A-G

55875784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76695899-G-A

55877351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76696293-G-T

55877458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76696894-T-C

55877458-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76696894-T-G

55877509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76696942-A-G

55877518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76696946-G-A

http://identifiers.org/hco/4/GRCh38#55877696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76697115-C-A

55877696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76697115-C-T

55877697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76697116-G-A

55877762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76697173-G-A

55877878-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76697265-C-G

55877878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76697265-C-T

55877879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76697266-T-C

55877911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 76697293-C-T

55878006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: synonymous variant
orthologous variants: 76697388-T-C

55878006-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: stop gained
orthologous variants: 76697388-T-G

55878073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 76697455-A-G

55878091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76697473-A-G

55878164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76697529-A-G

55878191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76697556-C-T

http://identifiers.org/hco/4/GRCh38#55878204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76697564-C-A

55878243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76697595-G-T

55878317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76697681-A-G

55880590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76699448-A-G

55880602-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76699460-T-G

55880603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76699461-C-T

55880616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76699474-T-C

55880617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76699475-T-C

55880779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76699686-A-G

55880841-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76699749-T-A

55881059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron variant
orthologous variants: 76700167-A-G

55882987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76701250-C-T

55883189-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76701401-C-G

55883274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76701471-A-G

http://identifiers.org/hco/4/GRCh38#55883327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76701530-C-A

55883409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76701590-G-T

55883555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76701707-G-A

55883555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76701707-G-T

55883582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76701733-T-C

55883615-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76701750-G-T

55883708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76701852-A-G

55883755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76701882-G-A

55883760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76701883-T-C

55884164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76702236-C-T

55884257-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76702331-T-A

55884350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76702395-T-C

55884386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76702433-A-G

55884958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76702925-T-C

55884958-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76702925-T-G

55884971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76702938-A-G

55885231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76703185-A-G

55885382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76703246-T-C

55886719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76703753-T-C

55886849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76703823-A-G

55886940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76703910-C-T

55886973-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76703943-A-T

55887360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76704411-A-G

55887523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76704559-A-G

55887629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76704604-C-T

55887955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76704795-A-G

55888348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76705164-T-C

55888409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76705213-A-G

55888523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76705314-C-T

55888919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 76705697-A-G

55888940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 76705718-T-C

55889176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76706032-A-G

55889204-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76706086-C-G

55889232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76706159-G-A

55889296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76706224-T-C

55889693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76706399-G-A

http://identifiers.org/hco/4/GRCh38#55890102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76706745-C-A

55890102-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76706745-C-G

55890102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76706745-C-T

55890171-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76706801-T-A

55890171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76706801-T-C

55890171-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76706801-T-G

55890206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76706834-G-A

55890399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76707022-A-G

55890492-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76707095-T-A

55890492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76707095-T-C

55890492-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76707095-T-G

55890654-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76707252-T-G

55890916-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76707283-T-A

55891069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76707344-A-G

55891167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76707428-G-A

55891167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76707428-G-T

55891215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76707467-T-C

55891225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76707478-G-A

55891225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76707478-G-T

55891246-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76707499-A-T

http://identifiers.org/hco/4/GRCh38#55891282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76707534-C-A

55891282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76707534-C-T

55891284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76707536-T-C

55891288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76707540-T-C

55892664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 76708206-A-G

55892719-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 76708261-T-G

http://identifiers.org/hco/4/GRCh38#55892829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76708746-C-A

http://identifiers.org/hco/4/GRCh38#55892845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76708762-C-A

55892845-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76708762-C-G

http://identifiers.org/hco/4/GRCh38#55892851-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76708768-A-C

55892880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76708787-A-G

http://identifiers.org/hco/4/GRCh38#55893477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76709059-C-A

55893477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76709059-C-T

http://identifiers.org/hco/4/GRCh38#55893696-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#76709283-A-C

55893696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 76709283-A-G

55893696-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 76709283-A-T

55895997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76710722-C-T

55896035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76710759-G-A

55896120-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76710839-T-G

55896679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76711037-T-C

http://identifiers.org/hco/4/GRCh38#55896996-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76711355-A-C

55896996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76711355-A-G

55896996-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76711355-A-T

55899018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76714285-G-A

55899494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76714675-G-A

55899654-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76714773-T-A

55899654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76714773-T-C

55899941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76715059-G-A

55899945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76715063-A-G

http://identifiers.org/hco/4/GRCh38#55900008-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76715113-A-C

55900008-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76715113-A-T

55900094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76715191-T-C

http://identifiers.org/hco/4/GRCh38#55900142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76715246-C-A

55900439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76715480-C-T

55902180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76715684-G-A

55902241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76715744-G-T

55902412-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 76715882-T-G

55902511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 76715981-T-C

55902674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76716203-G-A

55902674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76716203-G-T

55903037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76716387-G-A

55903066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76716412-C-T

55903119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76716465-A-G

55903260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76716531-G-A

55903267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76716538-A-G

55903318-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76716553-C-G

55903318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76716553-C-T

55903348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76716580-A-G

55903380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76716609-T-C

55903632-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76716806-C-G

55903962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76717100-A-G

55904012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76717150-A-G

55904045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76717181-G-A

55904223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76717346-A-G

55904229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76717352-G-A

55904229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76717352-G-T

http://identifiers.org/hco/4/GRCh38#55904249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76717372-C-A

55904249-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76717372-C-G

55904249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76717372-C-T

55904270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76717393-T-C

http://identifiers.org/hco/4/GRCh38#55904378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76717500-C-A

55904378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 76717500-C-T

55904384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 76717506-T-C

55904384-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 76717506-T-G

55904423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 76717545-A-G

55904516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76717637-A-G

http://identifiers.org/hco/4/GRCh38#55904555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76717674-C-A

55904577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76717696-G-A

55904613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76717730-G-A

55904613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76717730-G-T

http://identifiers.org/hco/4/GRCh38#55904671-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76717786-A-C

55904671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76717786-A-G

55904678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76717793-T-C

55904755-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76717866-T-A

55904755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76717866-T-C

55904756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76717867-G-T

55904775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76717886-A-G

55904786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76717896-G-A

55904786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76717896-G-T

55904796-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76717908-G-C

55904796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76717908-G-T

55904866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76717976-A-G

55904933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76718051-G-A

55904933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76718051-G-T

http://identifiers.org/hco/4/GRCh38#55904948-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76718066-A-C

55904948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76718066-A-G

55904981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30380
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76718098-C-T