76681846-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5284211-C-G

76681846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5284211-C-T

76681943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5284315-G-A

76682040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5284398-G-A

http://identifiers.org/hco/8/GRCh38#76682259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5284605-C-A

76682357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5284693-G-A

76682442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5284774-G-T

76682484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5284809-G-A

76682484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5284809-G-T

http://identifiers.org/hco/8/GRCh38#76682529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5284852-C-A

76682529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5284852-C-T

76682539-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5284862-C-G

76682539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5284862-C-T

76682571-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5284892-T-A

76682619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5284932-G-A

76682619-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5284932-G-C

76682619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5284932-G-T

http://identifiers.org/hco/8/GRCh38#76682712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5285038-C-A

76682712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5285038-C-T

76682750-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5285107-C-G

76682750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5285107-C-T

76682756-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5285113-A-T

76682904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5285586-T-C

76682992-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5285674-T-A

76682992-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5285674-T-G

76683053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 5285731-T-C

76683151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5285827-G-A

76683151-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5285827-G-C

76683151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5285827-G-T

76683177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 5285855-C-T

76683222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5285900-G-A

76683222-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5285900-G-C

http://identifiers.org/hco/8/GRCh38#76683242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5285920-C-A

http://identifiers.org/hco/8/GRCh38#76683243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5285921-C-A

76683243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5285921-C-T

http://identifiers.org/hco/8/GRCh38#76683245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5285923-C-A

76683245-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5285923-C-G

76683246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5285924-G-A

76683246-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5285924-G-C

76683246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5285924-G-T

76683284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5285959-A-G

http://identifiers.org/hco/8/GRCh38#76683315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5286001-C-A

76683315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5286001-C-T

http://identifiers.org/hco/8/GRCh38#76683321-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5286007-A-C

76683321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5286007-A-G

76683321-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5286007-A-T

http://identifiers.org/hco/8/GRCh38#76683383-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5286052-A-C

76683383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5286052-A-G

76683546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5286210-C-T

76683626-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5286290-G-C

76683628-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5286292-G-C

76683632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5286296-A-G

76683634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5286298-G-A

76683634-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5286298-G-C

76683634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5286298-G-T

76683703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5286371-G-T

76683704-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5286372-T-G

http://identifiers.org/hco/8/GRCh38#76683841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5286625-C-A

76683841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5286625-C-T

76683853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5286637-G-T

76684044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5286853-T-C

76684051-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5286860-T-G

76684194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5287015-C-T

76684200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5287021-C-T

76684686-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5287507-T-G

http://identifiers.org/hco/8/GRCh38#76684738-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5287556-A-C

76684833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5287649-G-A

76686201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5289019-G-A

76686606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5289442-G-A

76686815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5289650-G-A

http://identifiers.org/hco/8/GRCh38#76686839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5289674-C-A

76686859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5289694-G-A

76686895-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5289730-C-G

76687018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5289879-T-C

76688058-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5290930-C-G

76688058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5290930-C-T

76688753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5291625-T-C

http://identifiers.org/hco/8/GRCh38#76688799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5291671-C-A

76688799-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5291671-C-G

76688799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5291671-C-T

76688919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5291790-A-G

76689049-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5291920-T-G

http://identifiers.org/hco/8/GRCh38#76689117-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5291988-A-C

76689324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5292201-A-G

76690070-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5292914-T-A

76690734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5293947-C-T

76690937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5294134-G-A

76690950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5294147-G-A

76690951-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5294148-A-T

76690996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5294190-T-C

76691147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5294329-T-C

76691319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5294523-G-T

76691502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5294702-A-G

76691785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5294951-A-G

76691910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5295048-G-A

76692048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5295119-G-A

76692088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5295139-A-G

http://identifiers.org/hco/8/GRCh38#76692218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5295265-C-A

76692218-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5295265-C-G

76693109-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5295918-T-A

76693109-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5295918-T-G

76693269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5296040-A-G

76693473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5296233-A-G

76693572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5296339-T-C

76693794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5296638-G-A

http://identifiers.org/hco/8/GRCh38#76693925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5296774-C-A

76693925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5296774-C-T

76694039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5296886-C-T

76694170-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5297015-C-G

76694320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5297158-A-G

76694570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5297393-G-T

76694756-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5297486-T-G

76695880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5298631-G-A

76696024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5298775-G-A

76696340-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5299091-T-A

76696385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5299136-G-A

76696744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5299505-A-G

76696744-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5299505-A-T

76696989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5299747-G-A

76697130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5299869-C-T

76697335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5300115-T-C

76697411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5300186-T-C

76697825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5300598-G-A

76697882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5300646-G-T

76697924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5300688-A-G

76698025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5300776-A-G

76698054-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5300804-T-A

76698151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5300901-G-A

76698181-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5300931-A-T

76698493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5301240-T-C

76698696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5301442-A-G

76700556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5303295-G-A

http://identifiers.org/hco/8/GRCh38#76700610-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5303353-A-C

76701271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5304007-G-A

76701871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5304607-G-A

76701871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5304607-G-T

76702039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5304767-G-A

76702039-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5304767-G-T

http://identifiers.org/hco/8/GRCh38#76702040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5304768-C-A

76702120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5304845-C-T

76702185-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5304909-C-G

76702339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5305027-C-T

76702616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5305312-T-C

76702628-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5305324-A-T

76702664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5305363-C-T

http://identifiers.org/hco/8/GRCh38#76703148-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5305816-A-C

76703170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5305838-T-C

76703261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5305920-G-A

76703261-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5305920-G-T

76703337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5305997-A-G

76703444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5306104-A-G

76703482-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5306142-T-A

76703482-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5306142-T-G

76703686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5306371-T-C

76703770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5306454-G-A

76703814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5306497-G-A

76703922-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5306609-G-T

http://identifiers.org/hco/8/GRCh38#76704439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5307123-C-A

76704439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 5307123-C-T

76704505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 5307189-A-G

76704634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 5307318-T-C

76704634-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 5307318-T-G

76705204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 5307888-T-C

http://identifiers.org/hco/8/GRCh38#76705243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5307927-C-A

76705243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 5307927-C-T

76705244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5307928-G-A

76705244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5307928-G-T

76705257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5307941-G-A

http://identifiers.org/hco/8/GRCh38#76705280-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5307964-A-C

76705280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5307964-A-G

76705441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 5308125-C-T

76705654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 5308338-C-T

76705728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5308415-G-A

76705729-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5308416-T-A

76705729-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5308416-T-G

76705798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 5308485-A-G

76705954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5308635-G-T

76706401-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 5309082-T-G

76706536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 5309217-G-A

76706536-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 5309217-G-C

76706581-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 5309262-G-C

76706581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 5309262-G-T

http://identifiers.org/hco/8/GRCh38#76706587-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5309268-A-C

http://identifiers.org/hco/8/GRCh38#76706608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5309289-C-A

76706608-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 5309289-C-G

76706608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 5309289-C-T

http://identifiers.org/hco/8/GRCh38#76706612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5309293-C-A

76706612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5309293-C-T

76706666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5309347-G-A

76706712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5309390-G-A

76706712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5309390-G-T

76706788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5309452-T-C

76707086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5309742-T-C

76707458-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5310114-T-A

76707538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 5310195-T-C

76707553-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 5310210-T-A

76707553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 5310210-T-C

76708030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 5310687-G-A

76708030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 5310687-G-T

76708064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5310721-C-T

76708065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5310722-A-G

76708164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5310802-G-A

76708164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5310802-G-T

http://identifiers.org/hco/8/GRCh38#76708299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5310927-C-A

http://identifiers.org/hco/8/GRCh38#76708300-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5310928-A-C

http://identifiers.org/hco/8/GRCh38#76708301-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5310929-A-C

76708301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5310929-A-G

76708549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5311164-C-T

76709384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5311988-A-G

76709460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5312062-A-G

http://identifiers.org/hco/8/GRCh38#76709483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5312089-C-A

76709547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5312155-G-A

76709817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5312396-G-T

76709910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5312489-C-T

76709941-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5312524-T-A

76710942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5313533-T-C

76711265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5313896-A-G

76711297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5313927-T-C

76711839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5314477-G-A

http://identifiers.org/hco/8/GRCh38#76711872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5314507-C-A

76712196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5314816-T-C

76712653-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5315246-A-T

76712667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5315260-C-T

76712769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5315358-C-T

http://identifiers.org/hco/8/GRCh38#76712935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5315513-C-A

http://identifiers.org/hco/8/GRCh38#76713170-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5315736-A-C

76713567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5316021-T-C

76713853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5316296-G-T

http://identifiers.org/hco/8/GRCh38#76713989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5316402-C-A

76714141-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5316564-G-C

76714279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5316687-T-C

76714385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5316793-A-G

76715985-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5318540-G-C

76716001-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5318554-G-T

76716008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5318561-G-A

76716049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5318603-G-A

76716206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5318732-T-C

http://identifiers.org/hco/8/GRCh38#76716322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5318851-C-A

76716531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5319024-G-T

76716711-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5319244-T-G

76716743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5319271-T-C

76716754-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5319282-C-G

76716754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5319282-C-T

76717055-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5319564-C-G

76717436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5320099-T-C

76718001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5320318-T-C

76718091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5320403-C-T

76718536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5320879-T-C

76718561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5320904-A-G

76718615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5321266-C-T

76718656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5321308-T-C

76718789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5321438-A-G

76719197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5321826-G-A

76719206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5321835-G-T

76719322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5321943-A-G

76719379-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5321996-C-G

76719379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5321996-C-T

76719560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5322154-A-G

76719732-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5322313-G-C

76719952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5322497-G-A

76719959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5322507-G-A

76720298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5322824-C-T

76720873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5323476-A-G

76720960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5323555-C-T

76721324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5323915-G-A

76721359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5323950-T-C

76721521-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5324109-A-T

76721542-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5324128-T-A

76721591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5324171-T-C

76721850-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5324345-T-G

76721927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5324411-T-C

76722142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5324624-T-C

http://identifiers.org/hco/8/GRCh38#76722149-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5324631-A-C

76722189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5324671-A-G

76722267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5324743-A-G

76722604-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5325077-T-A

76722665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5325134-A-G

76722698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5325177-G-A

76722973-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5325418-G-C

76723088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5325548-T-C

76723257-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5325704-T-G

http://identifiers.org/hco/8/GRCh38#76723322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5325769-C-A

76723362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5325807-C-T

76723439-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5325872-T-G

76723477-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5325912-T-G

76723813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5326296-A-G

http://identifiers.org/hco/8/GRCh38#76724129-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5326719-A-C

76724183-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5326831-G-C

76724383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5327082-A-G

76724542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5327271-G-T

76724635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5327477-G-T

76724640-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5327482-T-G

76724882-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5327763-T-G

76725011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5327864-G-A

76725061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5327923-C-T

76725076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5327938-G-T

76725089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5327951-G-A

76725251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5328145-T-C

76725320-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5328203-T-G

76725371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5328252-C-T

76725378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5328259-G-T

76725397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5328278-C-T

76725452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5328332-C-T

76725463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5328343-C-T

76725539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5328406-G-A

http://identifiers.org/hco/8/GRCh38#76725566-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5328437-A-C

76725712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5328602-G-A

76725812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5328695-C-T

76725942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5328778-G-T

76726438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5329310-C-T

76726449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5329322-G-A

76726502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5329375-G-A

76726519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5329392-G-A

76726747-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5329780-T-G

76726785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5329818-C-T

76726978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5330039-A-G

76726995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5330056-G-A

76727209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5330269-G-A

76727234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5330294-G-A

76727234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5330294-G-T

76727267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5330325-G-A

76727269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5330327-C-T

http://identifiers.org/hco/8/GRCh38#76727424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5330488-C-A

76727428-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5330492-A-T

76727589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5330639-A-G

76727604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5330654-G-T

76728085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5331122-C-T

76728288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5332818-G-A

http://identifiers.org/hco/8/GRCh38#76728387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5332917-C-A

76728496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5333028-G-A

76728620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5333150-G-A

76728747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5333273-G-A

76728747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5333273-G-T

76728921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5333453-G-A

76729061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5333581-G-A

76729065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5333585-G-A

76729257-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5333750-T-A

76729257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5333750-T-C

76729589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5334036-C-T

76729665-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5334111-T-A

76729857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5334303-G-T

76729909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5334356-A-G

76730163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5334621-C-T

76730347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5334798-A-G

76730889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5335127-C-T

http://identifiers.org/hco/8/GRCh38#76730992-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5335230-A-C

76730992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5335230-A-G

76731091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5335317-C-T

76731301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5335498-A-G

76731340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5335537-C-T

76731341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5335538-G-A

76731341-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5335538-G-C

76731383-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5335578-T-A

76731529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5335715-A-G

76731623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5335798-T-C

76731832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5335939-T-C

76731890-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5336005-A-T

76732562-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5336454-C-G

76732886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5336889-C-T

76732962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5336965-G-A

76733156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5337145-G-A

76733156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5337145-G-T

76733331-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5337322-C-G

76733331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5337322-C-T

76733371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5337356-G-A

76733371-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5337356-G-C

76733371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5337356-G-T

76733620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5337540-A-G

76734293-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5338223-A-T

76734304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5338234-G-A

76734382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5338316-A-G

http://identifiers.org/hco/8/GRCh38#76734532-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5338662-A-C

76734847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5338976-C-T

http://identifiers.org/hco/8/GRCh38#76734885-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5339008-A-C

76734950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5339063-A-G

76734959-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5339072-T-A

76734965-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5339078-G-T

76734996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5339122-A-G

76735020-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5339146-A-T

http://identifiers.org/hco/8/GRCh38#76735166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5339289-C-A

76735166-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5339289-C-G

76735328-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5339442-A-T

76735784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5339898-C-T

76735871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5339985-A-G

76736288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5340381-G-A

76736331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5340423-T-C

76736657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5340749-C-T

76736745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5340843-G-A

76736815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5341357-A-G

76737380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5341635-G-A

76738090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5342337-C-T

76738274-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5342528-G-C

76738346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5342599-T-C

76738521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5342754-A-G

http://identifiers.org/hco/8/GRCh38#76738526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5342759-C-A

76738530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5342763-G-A

76738532-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5342765-C-G

76738542-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5342775-T-G

76738633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5342826-T-C

76738664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5342857-T-C

76738666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5342859-C-T

76738692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5342885-C-T

76738694-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5342887-C-G

76739115-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5343372-C-G

76739252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5343514-T-C

76739273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5343535-A-G

76739343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5343572-A-G

76739752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5343888-T-C

76740222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5344343-T-C

76740361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5344536-G-A

76740361-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5344536-G-C

76740369-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5344544-A-T

76740482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5344712-A-G

76740485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5344715-A-G

76740520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5344752-G-A

76740853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5345108-G-A

http://identifiers.org/hco/8/GRCh38#76740926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5345175-C-A

76741054-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5345302-A-T

76741608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5345762-G-A

76742066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5346219-T-C

76742458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5346611-A-G

76742489-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5346642-G-C

76742567-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5346717-T-G

http://identifiers.org/hco/8/GRCh38#76743100-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5347327-A-C

http://identifiers.org/hco/8/GRCh38#76743149-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5347377-A-C

76743780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5347977-G-A

76743780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5347977-G-T

http://identifiers.org/hco/8/GRCh38#76743899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5348058-C-A

76743906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5348065-A-G

http://identifiers.org/hco/8/GRCh38#76746885-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5352059-A-C

76746885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5352059-A-G

76747040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5352264-G-A

76747040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5352264-G-T

76747219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5352445-T-C

76747557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5352546-A-G

76748323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5352839-C-T

76749029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5353201-G-A

76749489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5353626-A-G

76750008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5354132-G-A

http://identifiers.org/hco/8/GRCh38#76750029-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5354162-A-C

76750395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5354487-T-C

76751143-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5355025-T-A

76751236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5355120-C-T

76751571-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5355469-G-C

http://identifiers.org/hco/8/GRCh38#76751793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5355650-C-A

76751812-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5355669-T-A

76755120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5363718-T-C

http://identifiers.org/hco/8/GRCh38#76755223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5363792-C-A

76755817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5364200-A-G

76756456-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5365778-T-A

76756541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5365841-T-C

76756947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5366189-C-T

http://identifiers.org/hco/8/GRCh38#76757259-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5366371-A-C

76757388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5366429-T-C

76757431-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5366462-C-G

76757963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5366910-T-C

76758073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5367023-T-C

76758077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5367027-T-C

76758111-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5367061-C-G

76758919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5367454-C-T

76758936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5367471-T-C

76759048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5367573-A-G

76759858-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5371317-T-A

76759858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5371317-T-C

76759860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5371319-C-T

76761469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5372804-A-G

76762507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5373766-G-A

76762762-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5374076-A-T

76762815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5374129-C-T

76762858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5374172-C-T

http://identifiers.org/hco/8/GRCh38#76763875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5376641-C-A

76764063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5376829-G-A

76764122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5376891-A-G

http://identifiers.org/hco/8/GRCh38#76764170-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5376944-A-C

76764192-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5376964-C-G

76764391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5377076-A-G

76764577-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5377237-T-A

76764856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5377468-C-T

76764953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5377552-A-G

76765039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5377628-G-A

http://identifiers.org/hco/8/GRCh38#76765168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5377756-C-A

76765497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5378059-A-G

76766189-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5378319-T-G

http://identifiers.org/hco/8/GRCh38#76766715-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5378817-A-C

76766826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5378926-A-G

76766968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5379017-C-T

76767037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5379078-A-G

76767037-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5379078-A-T

76767122-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5379132-A-T

76767504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5379506-A-G

http://identifiers.org/hco/8/GRCh38#76767697-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5379681-A-C

76767697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5379681-A-G

http://identifiers.org/hco/8/GRCh38#76767931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5379904-C-A

76768729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5380521-C-T

76771744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5387835-G-T

76771953-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5388039-G-C

76771962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5388048-G-T

76772153-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5388224-G-C

76772153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5388224-G-T

76772190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5388261-G-A

76772438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5388423-A-G

76772518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5388497-G-T

76772934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5388855-C-T

76773068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5388978-G-A

http://identifiers.org/hco/8/GRCh38#76773184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5389024-C-A

76773285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5389111-C-T

76773297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5389123-A-G

http://identifiers.org/hco/8/GRCh38#76773790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5389587-C-A

76774017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5389770-A-G

76774145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5389866-A-G

76774168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5389889-T-C

76774193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5389912-A-G

76774371-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5390104-A-T

76774542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5390269-T-C

76774886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5391316-C-T

76775788-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5392196-T-G

76775863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5392275-G-A

76776526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5392887-T-C

76776923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5393281-G-A

76776973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5393330-A-G

76777618-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5393972-T-A

76777618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5393972-T-C

76777795-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5394148-C-G

76777834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5394187-A-G

76777868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5394221-G-T

http://identifiers.org/hco/8/GRCh38#76778078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5394365-C-A

76778078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5394365-C-T

http://identifiers.org/hco/8/GRCh38#76778086-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5394373-A-C

http://identifiers.org/hco/8/GRCh38#76778243-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5394530-A-C

76778300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 5394587-G-A

76778300-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 5394587-G-C

76778549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5394816-T-C

76778837-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5395104-T-A

76779329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5395598-C-T

76779365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5395634-T-C

http://identifiers.org/hco/8/GRCh38#76780002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5396267-C-A

http://identifiers.org/hco/8/GRCh38#76780177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5396442-C-A

76780718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5396894-G-A

76780826-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5396976-C-G

http://identifiers.org/hco/8/GRCh38#76781014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5397157-C-A

http://identifiers.org/hco/8/GRCh38#76781286-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5397490-A-C

76781410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5397756-G-A

76782064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5398347-T-C

76782117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5398377-T-C

76782253-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5398507-T-G

http://identifiers.org/hco/8/GRCh38#76782573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5398818-C-A

76783183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5399395-A-G

76783253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5399453-G-A

76783362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5399543-G-T

76783408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5399586-A-G

76784149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5400267-C-T

76784166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5400284-G-A

76784621-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5400694-T-G

76784702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5400771-A-G

76784768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5400826-A-G

76784772-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5400830-T-G

76784780-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5400838-A-T

76785063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5401113-A-G

76785063-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5401113-A-T

76785220-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5401274-T-A

76785308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5401362-T-C

76785347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5401384-G-A

76786286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5401757-G-A

76786399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5401857-G-T

http://identifiers.org/hco/8/GRCh38#76786570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5401987-C-A

76786761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5402253-C-T

http://identifiers.org/hco/8/GRCh38#76786890-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5402370-A-C

76787180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5402571-G-A

76787229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5402632-T-C

76787345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5402748-G-A

76787379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5402779-G-A

76787379-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5402779-G-C

76787480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5402878-G-A

76787480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5402878-G-T

76787901-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5402944-T-A

76787922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5402963-T-C

76788156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5403169-T-C

http://identifiers.org/hco/8/GRCh38#76788433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5403472-C-A

76788588-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5403661-A-T

76789093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5404160-G-T

76789100-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5404167-G-C

76789623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5404666-C-T

76789736-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5404731-A-T

76789742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5404737-G-A

76789964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5404925-A-G

76790094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5405059-G-T

76790173-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5405144-T-A

http://identifiers.org/hco/8/GRCh38#76790234-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5405269-A-C

http://identifiers.org/hco/8/GRCh38#76790451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5405559-C-A

76790696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5405790-T-C

76790746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5405835-T-C

76790888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5405974-G-A

76791112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5406225-A-G

76791467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5406479-G-A

76791617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5406614-G-A

76791726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5406708-A-G

http://identifiers.org/hco/8/GRCh38#76791783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5406770-C-A

76791783-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5406770-C-G

76791931-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5406921-T-A

76792056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5407044-A-G

76792409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5407361-G-T

76792490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5407458-A-G

76792814-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5407778-T-A

http://identifiers.org/hco/8/GRCh38#76792821-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5407784-A-C

76793124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5408086-A-G

76793360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5408340-T-C

76793476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5408454-C-T

76793572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5408543-G-A

http://identifiers.org/hco/8/GRCh38#76793597-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5408560-A-C

76794210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5409165-T-C

76794340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5409278-T-C

76794460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5409398-T-C

76794644-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5409567-T-A

76794775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5409660-A-G

76794959-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5409819-T-G

76794968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5409827-A-G

76795243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5410054-A-G

76795243-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5410054-A-T

76795818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5410142-T-C

76796204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5410527-A-G

76796325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5410620-A-G

76796443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5410752-G-T

http://identifiers.org/hco/8/GRCh38#76796538-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5410838-A-C

76796538-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5410838-A-T

76796809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5411105-A-G

76796883-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5411181-T-A

76796883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5411181-T-C

76797242-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5411509-G-C

76797748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5411993-T-C

76797748-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5411993-T-G

76797808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5412053-G-A

76797842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5412087-G-A

76798307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5412550-C-T

76798395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5412638-G-A

76799817-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5414177-A-T

76799821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5414181-C-T

76799822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5414182-G-A

76799851-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5414207-T-G

76800739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5415066-C-T

76800838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5415165-C-T

76801538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5415918-A-G

76801712-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5416090-G-C

76801733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5416111-G-A

76801765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5416143-G-T

http://identifiers.org/hco/8/GRCh38#76802432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5416809-C-A

76802432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5416809-C-T

76802620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5416997-A-G

76802667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5417046-A-G

76802758-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5417126-C-G

76802758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5417126-C-T

76802870-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5417250-C-G

76803109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5417492-G-A

76803109-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5417492-G-C

76804773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5419321-G-A

76804773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5419321-G-T

76804876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5419447-C-T

76804877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5419448-G-A

76805318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5419897-G-A

76806103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5420703-A-G

76806121-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5420721-C-G

76806172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5420772-A-G

76806192-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5420789-T-G

76806348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5420941-G-T

76806801-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5421373-T-A

76807155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5421727-G-A

76808428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5422937-C-T

76809337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5423700-G-T

76809468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5423831-T-C

76809996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5424325-T-C

76809998-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5424327-G-C

http://identifiers.org/hco/8/GRCh38#76810149-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5424459-A-C

76810149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5424459-A-G

76810661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5425033-G-A

76810818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5425250-T-C

76810830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5425283-G-T

76810848-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5425301-G-C

76810972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5425422-C-T

76810983-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5425431-T-A

76811248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5425699-T-C

76812101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5426460-A-G

76812101-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5426460-A-T

76812189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5426584-T-C

76812470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5426891-T-C

76812476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5426897-G-A

76812534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5426946-G-A

76812648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5427052-T-C

76812710-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5427121-T-A

76813167-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5427587-T-A

76813603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5428018-A-G

76813697-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5428059-G-C

76813699-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5428061-A-T

http://identifiers.org/hco/8/GRCh38#76814685-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5428821-C-A

76814726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5428860-G-T

76815098-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5429184-C-G

76815305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5429360-A-G

76815316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5429371-T-C

76815338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5429393-A-G

76815440-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5429493-T-G

http://identifiers.org/hco/8/GRCh38#76815452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5429505-C-A

76815486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5429540-C-T

http://identifiers.org/hco/8/GRCh38#76815985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5429908-C-A

76816214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5430141-T-C

76819733-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5432714-T-A

76819733-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5432714-T-G

76820014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5432955-T-C

76820018-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5432959-A-T

76820132-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5433068-G-C

http://identifiers.org/hco/8/GRCh38#76820222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5433210-C-A

76820233-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5433222-A-T

76820350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5433353-C-T

76821551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5433520-G-A

76821551-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5433520-G-C

76821551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5433520-G-T

http://identifiers.org/hco/8/GRCh38#76821598-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5433568-A-C

76821710-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5433678-A-T

76821732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5433700-G-T

76821846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5433819-G-A

http://identifiers.org/hco/8/GRCh38#76822262-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5434170-A-C

76822284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5434192-A-G

76822397-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5434297-G-T

76822539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5434667-A-G

http://identifiers.org/hco/8/GRCh38#76822827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5435038-C-A

76823158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5435349-C-T

76823170-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5435361-T-A

76823185-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5435375-A-T

76823216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5435406-G-A

http://identifiers.org/hco/8/GRCh38#76823237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5435425-C-A

76823330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5435519-C-T

76823426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5435627-A-G

76823426-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5435627-A-T

76823560-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5435749-A-T

76823814-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5435973-A-T

76823913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5436019-A-G

http://identifiers.org/hco/8/GRCh38#76824106-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5436203-A-C

76824113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5436210-A-G

76825351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5437582-G-A

76825351-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5437582-G-C

76825351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5437582-G-T

76825473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5437708-C-T

76825646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5437864-T-C

76825857-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5439213-A-T

76825875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5439233-G-A

http://identifiers.org/hco/8/GRCh38#76827555-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5440726-A-C

http://identifiers.org/hco/8/GRCh38#76827676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5440846-C-A

76827676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5440846-C-T

76827743-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5440911-A-T

76827778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5440946-A-G

76827783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5440951-T-C

76827786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5440954-C-T

76827792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5440960-A-G

76828190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5441361-T-C

76828250-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5441420-T-A

http://identifiers.org/hco/8/GRCh38#76828889-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5442080-C-A

76828897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5442088-G-A

76828897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5442088-G-T

76829276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5442963-G-A

76829491-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5443126-T-G

76830110-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5443331-C-G

76830136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5443360-G-A

76830190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5443416-A-G

76830446-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5443665-T-G

http://identifiers.org/hco/8/GRCh38#76830613-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5443831-A-C

76830797-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5444014-T-G

76831018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5444241-T-C

76831108-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5444321-T-G

76831262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5444461-T-C

http://identifiers.org/hco/8/GRCh38#76831272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5444471-C-A

76831323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5444520-G-A

http://identifiers.org/hco/8/GRCh38#76831593-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5444791-C-A

76831609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5444804-T-C

76831648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5444816-G-A

76831669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5444836-T-C

http://identifiers.org/hco/8/GRCh38#76831967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5445119-C-A

76831967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5445119-C-T

76832017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5445186-A-G

76832050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5445219-A-G

76832050-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5445219-A-T

76832063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5445232-G-A

76832264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5445413-A-G

76832264-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5445413-A-T

76832280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5445428-T-C

76832550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5445710-G-A

76833001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5447302-C-T

http://identifiers.org/hco/8/GRCh38#76833212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5447498-C-A

76833212-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5447498-C-G

76833212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5447498-C-T

http://identifiers.org/hco/8/GRCh38#76833244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5447537-C-A

76833301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5447585-G-A

76833301-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5447585-G-T

76833399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 5447680-G-A

76833399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 5447680-G-T

http://identifiers.org/hco/8/GRCh38#76833417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5447696-C-A

76833417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5447696-C-T

76833424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5447702-T-C

76833463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5447741-T-C

http://identifiers.org/hco/8/GRCh38#76833515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5447791-C-A

76833577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5447831-T-C

76836505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5449160-G-A

76836654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5449307-G-A

76836654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5449307-G-T

76836721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5449368-G-A

76836721-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5449368-G-C

76836721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5449368-G-T

76836756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5449402-G-A

76836808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5449482-C-T

76837355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5449977-G-A

76837531-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5450163-A-T

76837574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5450171-T-C

76837765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5450395-C-T

76837807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5450427-T-C

76837864-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5450482-G-C

76837864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5450482-G-T

http://identifiers.org/hco/8/GRCh38#76837969-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5450584-A-C

76837991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5450606-A-G

76838180-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5450806-G-C

76838180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5450806-G-T

76838239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5450863-G-A

http://identifiers.org/hco/8/GRCh38#76838246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5450865-C-A

76838246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5450865-C-T

76838570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5451168-G-A

http://identifiers.org/hco/8/GRCh38#76838671-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5451268-A-C

http://identifiers.org/hco/8/GRCh38#76838692-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5451287-A-C

http://identifiers.org/hco/8/GRCh38#76839315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5452108-C-A

76839421-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5452224-T-A

76839421-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5452224-T-G

http://identifiers.org/hco/8/GRCh38#76839470-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5452273-A-C

76839470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5452273-A-G

76839645-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5452424-G-C

76839766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5452532-T-C

76839817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5452593-C-T

76840117-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5452887-T-A

76840376-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5453139-T-A

76840741-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5453500-T-A

76841001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5453747-T-C

76841139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5453871-C-T

76842005-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5454686-A-T

76842056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5454737-G-A

76842378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5455046-T-C

http://identifiers.org/hco/8/GRCh38#76842400-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5455068-A-C

76842400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5455068-A-G

76842488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5455217-T-C

76842545-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5455276-T-G

76842757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5455498-C-T

http://identifiers.org/hco/8/GRCh38#76842799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5455539-C-A

76843541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5456361-C-T

76843684-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5456500-T-A

76844085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5456891-G-T

76844199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5456988-C-T

76844413-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5457189-C-G

76844585-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5457388-C-G

76844674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5457464-T-C

76844702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5457492-T-C

76845299-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5458092-T-G

76845323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5458116-G-A

76845340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5458133-G-A

76845541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5458333-G-A

76845929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5458715-A-G

76846231-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5459022-T-A

76846962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5459482-C-T

76846963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5459483-G-A

76846988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5459507-C-T

76847078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5459593-C-T

76847095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5459610-G-A

http://identifiers.org/hco/8/GRCh38#76847431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5460096-C-A

76847632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5460258-C-T

76848206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5460859-C-T

76848647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5461297-A-G

http://identifiers.org/hco/8/GRCh38#76849002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5461638-C-A

76849004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5461640-C-T

76849087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5461720-A-G

76849087-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5461720-A-T

76849204-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5461835-A-T

76849235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5461854-G-T

76849335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5461894-C-T

http://identifiers.org/hco/8/GRCh38#76849554-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5462002-A-C

76849643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5462091-G-A

76849643-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5462091-G-C

http://identifiers.org/hco/8/GRCh38#76849744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5462192-C-A

76849744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5462192-C-T

http://identifiers.org/hco/8/GRCh38#76849773-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5462219-A-C

http://identifiers.org/hco/8/GRCh38#76849859-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5462306-A-C

76849931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5462380-T-C

76850269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5462762-C-T

76850286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 5462779-G-A

76850286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 5462779-G-T

http://identifiers.org/hco/8/GRCh38#76850483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5463338-C-A

76850747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5463588-A-G

76850842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5463679-G-A

76850842-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5463679-G-C

76850962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5463797-G-T

http://identifiers.org/hco/8/GRCh38#76851039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5463874-C-A

76851366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5464201-G-A

76851391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 5464226-G-A

76851429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5464264-G-A

76851634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 5464469-A-G

76851634-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5464469-A-T

76851826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 5464661-G-A

76851882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5464717-G-T

76851917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: missense_variant, undefined
orthologous variants: 5464752-G-A

76852189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: synonymous variant
orthologous variants: 5465027-G-A

76852189-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: missense variant
orthologous variants: 5465027-G-C

76852189-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: missense variant
orthologous variants: 5465027-G-T

http://identifiers.org/hco/8/GRCh38#76853038-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5465870-A-C

76853038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: synonymous variant
orthologous variants: 5465870-A-G

76853038-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: synonymous variant
orthologous variants: 5465870-A-T

http://identifiers.org/hco/8/GRCh38#76853050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5465882-C-A

76853050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: synonymous variant
orthologous variants: 5465882-C-T

http://identifiers.org/hco/8/GRCh38#76853053-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5465885-A-C

76853053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: synonymous variant
orthologous variants: 5465885-A-G

76853053-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: synonymous variant
orthologous variants: 5465885-A-T

76853275-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: synonymous variant
orthologous variants: 5466110-A-T

76853347-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: missense variant
orthologous variants: 5466182-A-T

76853551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: synonymous variant
orthologous variants: 5466386-A-G

76853560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: synonymous variant
orthologous variants: 5466395-C-T

76853680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: synonymous variant
orthologous variants: 5466515-T-C

76853704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: synonymous variant
orthologous variants: 5466539-T-C

76853812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: synonymous variant
orthologous variants: 5466647-A-G

76853854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: missense variant
orthologous variants: 5466689-G-T

76854001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: synonymous variant
orthologous variants: 5466836-A-G

76854018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: missense variant
orthologous variants: 5466853-T-C

76854076-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: synonymous variant
orthologous variants: 5466911-T-A

76854118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: synonymous variant
orthologous variants: 5466953-T-C

76854276-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: missense variant
orthologous variants: 5467102-C-G

76854307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: synonymous variant
orthologous variants: 5467133-T-C

76854379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: synonymous variant
orthologous variants: 5467205-A-G

http://identifiers.org/hco/8/GRCh38#76854670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5467496-C-A

76854670-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: missense variant
orthologous variants: 5467496-C-G

76854670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: synonymous variant
orthologous variants: 5467496-C-T

http://identifiers.org/hco/8/GRCh38#76854715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5467541-C-A

76854715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: synonymous variant
orthologous variants: 5467541-C-T

http://identifiers.org/hco/8/GRCh38#76854889-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5467715-A-C

76854889-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: synonymous variant
orthologous variants: 5467715-A-T

76854922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: synonymous variant
orthologous variants: 5467748-G-A

76854922-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: synonymous variant
orthologous variants: 5467748-G-T

76855424-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: missense variant
orthologous variants: 5468247-C-G

76855472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: missense variant
orthologous variants: 5468295-C-T

76855588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: synonymous variant
orthologous variants: 5468411-A-G

76855696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: synonymous variant
orthologous variants: 5468519-T-C

http://identifiers.org/hco/8/GRCh38#76855741-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5468564-A-C

76855741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: synonymous variant
orthologous variants: 5468564-A-G

76855810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: synonymous variant
orthologous variants: 5468633-G-A

76855810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: synonymous variant
orthologous variants: 5468633-G-T

76855861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: synonymous variant
orthologous variants: 5468684-A-G

76855981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: missense variant
orthologous variants: 5468804-G-T

76856095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: synonymous variant
orthologous variants: 5468918-G-A

76856143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: synonymous variant
orthologous variants: 5468966-G-A

http://identifiers.org/hco/8/GRCh38#76856188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5469011-C-A

http://identifiers.org/hco/8/GRCh38#76856307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5469130-C-A

http://identifiers.org/hco/8/GRCh38#76856396-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5469217-A-C

76856439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron variant
orthologous variants: 5469261-A-G

http://identifiers.org/hco/8/GRCh38#76856759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5469560-C-A

76856861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron variant
orthologous variants: 5469698-A-G

76857056-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron variant
orthologous variants: 5469881-T-A

76857457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron variant
orthologous variants: 5470207-A-G

76857514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron variant
orthologous variants: 5470263-A-G

76857523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron variant
orthologous variants: 5470270-T-C

76857594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron variant
orthologous variants: 5470339-G-A

76857594-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron variant
orthologous variants: 5470339-G-C

76857702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron variant
orthologous variants: 5470427-C-T

76857751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron variant
orthologous variants: 5470476-T-C

76857790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron variant
orthologous variants: 5470499-C-T

76858208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron variant
orthologous variants: 5470814-G-A

76858208-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron variant
orthologous variants: 5470814-G-C

76858442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron variant
orthologous variants: 5471052-G-T

76858627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron variant
orthologous variants: 5471242-G-A

76858674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron variant
orthologous variants: 5471288-A-G

76858764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron variant
orthologous variants: 5471372-A-G

76858822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron variant
orthologous variants: 5472302-T-C

76858964-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron variant
orthologous variants: 5472437-T-G

76859401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron variant
orthologous variants: 5472835-A-G

76859518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron variant
orthologous variants: 5472950-C-T

76859683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron variant
orthologous variants: 5473179-T-C

76859719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron variant
orthologous variants: 5473215-A-G

76859749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron variant
orthologous variants: 5473245-A-G

76860142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron variant
orthologous variants: 5473833-G-T

http://identifiers.org/hco/8/GRCh38#76860196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5473891-C-A

76860303-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron variant
orthologous variants: 5473971-A-T

76860455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron variant
orthologous variants: 5474110-C-T

76860551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron variant
orthologous variants: 5474192-G-A

76860589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron variant
orthologous variants: 5474234-A-G

http://identifiers.org/hco/8/GRCh38#76860676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5474302-C-A

76860938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron variant
orthologous variants: 5474487-C-T

76861135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron variant
orthologous variants: 5474634-T-C

76861529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron variant
orthologous variants: 5475002-G-A

76861598-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron variant
orthologous variants: 5475074-A-T

76861765-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron variant
orthologous variants: 5475457-C-G

76861893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron variant
orthologous variants: 5475585-T-C

76862098-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron variant
orthologous variants: 5475772-T-G

76862263-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron variant
orthologous variants: 5475931-A-T

76862345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron variant
orthologous variants: 5476003-G-A

76862596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron variant
orthologous variants: 5476270-G-A

76862950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron variant
orthologous variants: 5476611-G-T

76862969-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron variant
orthologous variants: 5476630-T-A

http://identifiers.org/hco/8/GRCh38#76863042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5476690-C-A

76863062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron variant
orthologous variants: 5476713-G-A

76863062-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: intron variant
orthologous variants: 5476713-G-C

76863203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: synonymous variant
orthologous variants: 5476851-A-G

http://identifiers.org/hco/8/GRCh38#76863260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5476902-C-A

76863260-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: synonymous variant
orthologous variants: 5476902-C-G

76863260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: synonymous variant
orthologous variants: 5476902-C-T

http://identifiers.org/hco/8/GRCh38#76863318-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5476960-A-C

76863318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: missense variant
orthologous variants: 5476960-A-G

76863326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: synonymous variant
orthologous variants: 5476968-G-A

76863335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: synonymous variant
orthologous variants: 5476977-A-G

76863359-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: missense variant
orthologous variants: 5477001-C-G

76863467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: synonymous variant
orthologous variants: 5477109-T-C

76863470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: synonymous variant
orthologous variants: 5477112-T-C

76863598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: missense variant
orthologous variants: 5477240-G-A

76863598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: missense variant
orthologous variants: 5477240-G-T

http://identifiers.org/hco/8/GRCh38#76863599-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5477241-C-A

76863599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: synonymous variant
orthologous variants: 5477241-C-T

http://identifiers.org/hco/8/GRCh38#76863811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5477453-C-A

76863811-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: missense variant
orthologous variants: 5477453-C-G

76863811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: missense variant
orthologous variants: 5477453-C-T

76864025-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: missense variant
orthologous variants: 5477667-G-C

76864618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: 3 prime UTR variant
orthologous variants: 5478260-A-G

76864618-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: 3 prime UTR variant
orthologous variants: 5478260-A-T

http://identifiers.org/hco/8/GRCh38#76865149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5478791-C-A

76865149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: 3 prime UTR variant
orthologous variants: 5478791-C-T

76865158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: 3 prime UTR variant
orthologous variants: 5478800-A-G

76865159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: 3 prime UTR variant
orthologous variants: 5478801-T-C

76865161-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: 3 prime UTR variant
orthologous variants: 5478803-G-C

76865161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: 3 prime UTR variant
orthologous variants: 5478803-G-T

76865465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: 3 prime UTR variant
orthologous variants: 5479107-G-A

76865465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: 3 prime UTR variant
orthologous variants: 5479107-G-T

76865737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: 3 prime UTR variant
orthologous variants: 5479382-A-G

76865737-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: 3 prime UTR variant
orthologous variants: 5479382-A-T

76865935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: 3 prime UTR variant
orthologous variants: 5479583-T-C

76865988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: 3 prime UTR variant
orthologous variants: 5479636-G-A

76865988-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: 3 prime UTR variant
orthologous variants: 5479636-G-T

76866202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: 3 prime UTR variant
orthologous variants: 5479851-G-T

76866413-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: 3 prime UTR variant
orthologous variants: 5480057-T-G

http://identifiers.org/hco/8/GRCh38#76866676-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5480312-A-C

76866676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: 3 prime UTR variant
orthologous variants: 5480312-A-G

http://identifiers.org/hco/8/GRCh38#76866707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#5480343-C-A

76866707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: 3 prime UTR variant
orthologous variants: 5480343-C-T

76866829-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30939
most severe consequence: 3 prime UTR variant
orthologous variants: 5480464-T-A