97756507-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36831444-A-T

http://identifiers.org/hco/2/GRCh38#97756542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36831478-C-A

http://identifiers.org/hco/2/GRCh38#97756551-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36831487-A-C

97756551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36831487-A-G

http://identifiers.org/hco/2/GRCh38#97756660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36831598-C-A

97756660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36831598-C-T

97756692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36831630-C-T

97756712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36831650-G-T

97756730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36831668-T-C

97756797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36831734-G-A

http://identifiers.org/hco/2/GRCh38#97756805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36831742-C-A

97756805-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36831742-C-G

http://identifiers.org/hco/2/GRCh38#97756869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36831798-C-A

97756869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36831798-C-T

97756946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36831875-G-A

97756946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36831875-G-T

97756950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36831879-G-A

97756950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36831879-G-T

97756987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36831898-A-G

http://identifiers.org/hco/2/GRCh38#97757016-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36831923-A-C

97757084-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36831986-T-G

97757218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36832121-T-C

97757240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36832143-G-A

97757240-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36832143-G-C

97757363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36832266-G-A

http://identifiers.org/hco/2/GRCh38#97757409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36832313-C-A

97757409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36832313-C-T

97758456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36832848-G-T

http://identifiers.org/hco/2/GRCh38#97758710-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36832990-A-C

97758710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36832990-A-G

97759025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36833257-T-C

97759027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 36833259-G-A

97759027-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36833259-G-C

97759127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36833337-C-T

http://identifiers.org/hco/2/GRCh38#97759174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36833383-C-A

http://identifiers.org/hco/2/GRCh38#97759223-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36833418-A-C

97759223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36833418-A-G

http://identifiers.org/hco/2/GRCh38#97759270-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36833441-A-C

http://identifiers.org/hco/2/GRCh38#97759327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36833496-C-A

97759401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36833565-G-A

97759401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36833565-G-T

97759433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36833596-A-G

97759436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36833599-G-A

97759443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36833606-G-A

97759443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36833606-G-T

http://identifiers.org/hco/2/GRCh38#97759689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36833922-C-A

97759689-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36833922-C-G

97759689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36833922-C-T

97759791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36834013-G-T

97759822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36834039-A-G

http://identifiers.org/hco/2/GRCh38#97759848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36834061-C-A

97759848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36834061-C-T

97760607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36834196-G-A

97760637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36834226-G-A

http://identifiers.org/hco/2/GRCh38#97760783-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36834367-A-C

97760851-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36834434-C-G

97760851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36834434-C-T

97761000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36834556-G-T

97761174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36834687-G-A

97761174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36834687-G-T

http://identifiers.org/hco/2/GRCh38#97761175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36834689-C-A

97761175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36834689-C-T

97761221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36834733-G-A

97761221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36834733-G-T

97761878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36835141-G-A

97761878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36835141-G-T

97761899-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36835158-T-A

97761899-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36835158-T-G

97762040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36835248-G-A

97762085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36835290-G-A

97762085-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36835290-G-C

97762105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36835310-G-A

97762105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36835310-G-T

http://identifiers.org/hco/2/GRCh38#97762307-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36835498-A-C

97762349-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36835535-G-C

97762349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36835535-G-T

97762358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36835544-G-A

97762358-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36835544-G-C

97762399-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36835589-G-C

97762399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36835589-G-T

97762447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36835631-T-C

97762449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36835633-T-C

http://identifiers.org/hco/2/GRCh38#97762453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36835637-C-A

97762453-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36835637-C-G

97762453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36835637-C-T

http://identifiers.org/hco/2/GRCh38#97762463-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36835644-A-C

97762463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36835644-A-G

http://identifiers.org/hco/2/GRCh38#97762464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36835645-C-A

97762464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36835645-C-T

97762533-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36835675-T-A

97762533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36835675-T-C

97762545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36835685-G-T

97762625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36835766-G-T

97762629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36835770-G-T

97764265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36837558-A-G

97764308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36837601-G-A

97764308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36837601-G-T

http://identifiers.org/hco/2/GRCh38#97764394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36837678-C-A

97764418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36837700-A-G

97764431-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36837704-C-G

97764431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36837704-C-T

97764471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36837740-G-A

97764471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36837740-G-T

97764492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36837761-A-G

http://identifiers.org/hco/2/GRCh38#97764548-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36837817-C-A

97764548-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36837817-C-G

97764548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36837817-C-T

97764580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36837838-A-G

97766163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: synonymous variant
orthologous variants: 36838072-G-A

97766178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: synonymous variant
orthologous variants: 36838087-T-C

97766178-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: synonymous variant
orthologous variants: 36838087-T-G

http://identifiers.org/hco/2/GRCh38#97766640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36838519-C-A

97766640-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36838519-C-G

97766640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36838519-C-T

http://identifiers.org/hco/2/GRCh38#97766690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36838572-C-A

97767770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36839316-T-C

97767786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36839340-C-T

97767812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36839367-C-T

97767940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36839513-A-G

97768112-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36839702-T-G

97768173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36839747-T-C

97768595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36840140-C-T

97771636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36840312-A-G

97771667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36840347-G-A

97771681-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36840359-T-A

97771923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36840604-T-C

97772138-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36840799-C-G

http://identifiers.org/hco/2/GRCh38#97772181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36840834-C-A

97772247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36840884-C-T

97772294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36840903-C-T

97772300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: missense variant
orthologous variants: 36840909-G-A

97772300-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: missense variant
orthologous variants: 36840909-G-C

97772371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: synonymous variant
orthologous variants: 36840980-T-C

97772469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36841077-G-T

97772493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36841102-A-G

97774948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36842295-A-G

97774999-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36842344-C-G

97775041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36842387-A-G

97775282-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36842610-C-G

97775282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36842610-C-T

97775366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36843165-G-A

http://identifiers.org/hco/2/GRCh38#97775401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36843202-C-A

97775425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 36843224-T-C

97775506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36843276-G-T

http://identifiers.org/hco/2/GRCh38#97775550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36843322-C-A

97775720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36843477-G-A

97775720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36843477-G-T

97775982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: missense variant
orthologous variants: 36843688-G-A

97775982-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: missense variant
orthologous variants: 36843688-G-C

97775996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: synonymous variant
orthologous variants: 36843702-G-A

97776409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36843799-G-A

97776594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36843959-G-A

97777008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36844224-A-G

97777068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36844272-T-C

http://identifiers.org/hco/2/GRCh38#97788618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36846364-C-A

97792260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36846859-A-G

97792286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36846879-G-A

97792286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36846879-G-T

97792296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36846888-T-C

97792325-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36846917-T-G

97792372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36846947-T-C

97792408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: synonymous variant
orthologous variants: 36846987-T-C

97792417-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: missense variant
orthologous variants: 36846996-C-G

97792417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: synonymous variant
orthologous variants: 36846996-C-T

97792515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: missense variant
orthologous variants: 36847094-T-C

http://identifiers.org/hco/2/GRCh38#97792560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36847139-C-A

97792560-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: missense variant
orthologous variants: 36847139-C-G

97792560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: missense variant
orthologous variants: 36847139-C-T

97792576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: synonymous variant
orthologous variants: 36847155-A-G

97792583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: missense variant
orthologous variants: 36847162-G-A

97792751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: missense variant
orthologous variants: 36847330-G-A

97792827-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: missense variant
orthologous variants: 36847406-C-G

97792827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: missense variant
orthologous variants: 36847406-C-T

97792837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: synonymous variant
orthologous variants: 36847416-G-A

97792837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: missense variant
orthologous variants: 36847416-G-T

http://identifiers.org/hco/2/GRCh38#97793085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36847652-C-A

97793085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36847652-C-T

97793086-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36847653-T-A

97793086-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36847653-T-G

97793094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36847657-G-A

97793094-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36847657-G-C

97793094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36847657-G-T

http://identifiers.org/hco/2/GRCh38#97793123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36847680-C-A

97793123-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36847680-C-G

97793123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36847680-C-T

http://identifiers.org/hco/2/GRCh38#97793172-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36847733-A-C

97793172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36847733-A-G

97793173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36847734-G-A

97793173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36847734-G-T

http://identifiers.org/hco/2/GRCh38#97793301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36847822-C-A

97793301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36847822-C-T

97793303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36847824-G-A

97793303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36847824-G-T

97793332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36847845-A-G

97793332-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36847845-A-T

97793684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36848181-A-G

97793728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36848216-C-T

97794445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36848893-G-T

97794762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36849205-G-A

97794795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36849241-A-G

97794795-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36849241-A-T

http://identifiers.org/hco/2/GRCh38#97794827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36849275-C-A

97794827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36849275-C-T

97794833-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36849281-T-A

97794854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36849301-G-A

97794854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36849301-G-T

97794902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36849345-A-G

97794941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36849373-T-C

97794941-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36849373-T-G

97794962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36849394-C-T

97795034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36849466-T-C

97795131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36849563-G-A

97795131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36849563-G-T

97795140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36849572-G-A

97795140-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36849572-G-C

97795140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36849572-G-T

97795666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36849845-T-C

97795673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36849852-T-C

97795720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36849898-C-T

http://identifiers.org/hco/2/GRCh38#97796079-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36850230-A-C

http://identifiers.org/hco/2/GRCh38#97796154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36850407-C-A

97796154-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36850407-C-G

97796154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36850407-C-T

97796181-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36850451-G-C

97796181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36850451-G-T

97796250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36850521-T-C

97796366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36850637-T-C

http://identifiers.org/hco/2/GRCh38#97796517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36850779-C-A

97796547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36850809-G-T

97796817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36851219-G-T

97796944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: synonymous variant
orthologous variants: 36851342-T-C

97797065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36851465-T-C

97797224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36851546-T-C

97797236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36851558-T-C

97797250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36851573-G-T

97797350-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36851624-T-A

97797350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36851624-T-C

97797557-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36851830-T-A

97797557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36851830-T-C

97797643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36851904-T-C

97797658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36851925-T-C

97797658-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36851925-T-G

97797674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36851938-C-T

97797842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36852099-A-G

97797848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36852105-C-T

97797998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36852235-G-A

http://identifiers.org/hco/2/GRCh38#97798074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36852295-C-A

97798217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36852418-G-T

97798349-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36852496-T-A

97798963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36852955-T-C

97798981-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36852972-C-G

97799233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36853172-A-G

97800900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36853610-T-C

97800944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36853653-A-G

97801163-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36853740-T-A

97801163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36853740-T-C

97801486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36854015-T-C

97801688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36854371-T-C

97801811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36854471-A-G

97801820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36854480-T-C

97801820-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36854480-T-G

http://identifiers.org/hco/2/GRCh38#97802099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36854725-C-A

97802099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36854725-C-T

http://identifiers.org/hco/2/GRCh38#97802279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36854890-C-A

97802279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36854890-C-T

http://identifiers.org/hco/2/GRCh38#97802301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36854912-C-A

97802301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36854912-C-T

97802438-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: missense variant
orthologous variants: 36854978-A-T

97802613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36855149-T-C

97802744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: missense variant
orthologous variants: 36855282-T-C

97802745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: missense variant
orthologous variants: 36855283-T-C

97803197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36855748-C-T

97803468-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36855991-T-G

97803484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36856007-C-T

97803809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36856254-C-T

97804127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36857176-A-G

97804251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36857293-T-C

97804300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36857338-C-T

97805048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36857705-T-C

97805231-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36857882-T-A

97805473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36858071-C-T

http://identifiers.org/hco/2/GRCh38#97805495-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36858095-A-C

97805497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36858097-G-A

97805758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36858316-G-T

97805829-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36858354-T-A

97805829-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36858354-T-G

http://identifiers.org/hco/2/GRCh38#97806080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36858576-C-A

97806465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36859459-C-T

http://identifiers.org/hco/2/GRCh38#97806662-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36859596-A-C

97806728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36859638-T-C

97806915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, undefined
orthologous variants: 36859781-C-T

97806935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron_variant, undefined
orthologous variants: 36859805-C-T

97809633-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36862101-T-G

97809660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36862128-A-G

http://identifiers.org/hco/2/GRCh38#97809665-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36862133-A-C

97809665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36862133-A-G

97809700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: synonymous variant
orthologous variants: 36862160-T-C

97809700-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: synonymous variant
orthologous variants: 36862160-T-G

97809802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36862266-T-C

97809893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36862357-T-C

http://identifiers.org/hco/2/GRCh38#97810016-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36862469-A-C

97810877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36863549-A-G

97810877-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36863549-A-T

97810883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36863555-T-C

97811209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: synonymous variant
orthologous variants: 36863878-A-G

97811214-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: missense variant
orthologous variants: 36863883-A-T

http://identifiers.org/hco/2/GRCh38#97811255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36863923-C-A

97811255-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36863923-C-G

97811255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36863923-C-T

97812424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: synonymous variant
orthologous variants: 36864296-T-C

97812445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: synonymous variant
orthologous variants: 36864317-T-C

97812469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: synonymous variant
orthologous variants: 36864341-A-G

97812973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36864701-C-T

97813081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36864760-G-T

97813235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36864868-G-A

http://identifiers.org/hco/2/GRCh38#97813518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36865083-C-A

97813914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36866055-T-C

97813914-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36866055-T-G

97814121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: synonymous variant
orthologous variants: 36866242-T-C

97814126-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: missense variant
orthologous variants: 36866247-T-G

97814179-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: intron variant
orthologous variants: 36866291-G-C

97814256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: synonymous variant
orthologous variants: 36866364-T-C

97814286-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: synonymous variant
orthologous variants: 36866394-C-G

97814286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: synonymous variant
orthologous variants: 36866394-C-T

97814304-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: synonymous variant
orthologous variants: 36866412-A-T

97814361-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 36866469-T-A

http://identifiers.org/hco/2/GRCh38#97814458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36866552-C-A

97814570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36866662-A-G

97814928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36866911-T-C

http://identifiers.org/hco/2/GRCh38#97815196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36867143-C-A

97815196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36867143-C-T

97815231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 36867178-A-G

97815246-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 36867193-C-G

97815246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 36867193-C-T

97815303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, missense_variant, synonymous_variant
orthologous variants: 36867250-C-T

http://identifiers.org/hco/2/GRCh38#97815353-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36867519-A-C

97815389-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36867559-T-A

97815389-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36867559-T-G

97815452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36867604-T-C

97815452-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36867604-T-G

http://identifiers.org/hco/2/GRCh38#97815507-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36867649-A-C

97818310-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36868388-A-T

97818349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36868420-C-T

97818439-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36868500-G-C

97818552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36868589-G-T

97819044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36869006-G-A

97819321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36869256-G-A

97819321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36869256-G-T

http://identifiers.org/hco/2/GRCh38#97819481-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36869471-A-C

97819846-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36869975-C-G

97819916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36870034-T-C

97820235-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36870333-T-G

97820237-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36870335-G-C

97820405-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36870507-T-A

97820438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36870527-G-A

97820486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36870560-G-T

97820499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36870569-G-A

97820529-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36870588-T-A

97820529-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36870588-T-G

http://identifiers.org/hco/2/GRCh38#97829895-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36870829-A-C

97830169-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36871084-T-A

97830507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36871616-A-G

97830507-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36871616-A-T

97830595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36871695-T-C

97830734-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36871806-T-G

97830826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36871886-C-T

97830888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36871963-C-T

97831139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36872172-C-T

97831164-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36872197-C-G

97831206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36872219-T-C

97831339-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36872307-G-C

97833216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36872417-G-A

97833344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36872556-A-G

97833437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36872649-T-C

97833437-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36872649-T-G

97833441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36872653-G-A

97833441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36872653-G-T

97834134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36872809-A-G

97834309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36872926-C-T

97834729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36873805-A-G

http://identifiers.org/hco/2/GRCh38#97834743-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36873812-A-C

97834748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36873817-T-C

97834748-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36873817-T-G

97834760-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36873829-C-G

97834797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 36873865-A-G

97834863-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 36873931-A-T

97834938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36874005-C-T

97834964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36874030-T-C

97834971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36874037-G-T

97834977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36874043-C-T

http://identifiers.org/hco/2/GRCh38#97835005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36874070-C-A

97835005-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36874070-C-G

97835005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36874070-C-T

http://identifiers.org/hco/2/GRCh38#97835009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36874074-C-A

97835026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36874094-T-C

97835091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36874176-T-C

http://identifiers.org/hco/2/GRCh38#97835098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36874183-C-A

97835131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36874220-G-T

97835245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36874334-T-C

97835354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36874429-C-T

http://identifiers.org/hco/2/GRCh38#97835734-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36874655-A-C

97837308-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36877201-T-A

97837452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36877309-T-C

97837464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36877321-C-T

97837951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36878464-T-C

97838069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36878617-T-C

97838476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36879081-G-A

97841782-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36879430-G-C

http://identifiers.org/hco/2/GRCh38#97841801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36879445-C-A

97841801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36879445-C-T

97841940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 36879595-G-A

97841940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 36879595-G-T

97841954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36879609-A-G

97842027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36879680-A-G

http://identifiers.org/hco/2/GRCh38#97842096-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36879722-A-C

97842125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36879744-A-G

97842515-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36880085-T-A

97842665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36880216-T-C

97842830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36880382-G-A

97844106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36880639-A-G

97844126-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36880657-T-A

97844285-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36880819-T-A

97844285-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36880819-T-G

97844726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36881247-A-G

97844805-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36881305-T-G

97844938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36881430-T-C

97845439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36881807-G-A

97845667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36882015-G-A

97845671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36882019-C-T

97855822-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36890861-T-A

97855840-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36890879-C-G

97857207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36891693-T-C

97857242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36891726-G-A

97857252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36891736-C-T

97857305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36891773-G-A

97857495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36891920-T-C

http://identifiers.org/hco/2/GRCh38#97857692-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36892097-A-C

97858122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36892719-G-A

97858156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36892751-T-C

97858259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36892849-C-T

97858320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36892907-T-C

97858720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36893218-T-C

97858732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36893231-G-T

97858781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36893267-C-T

97858840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36893325-T-C

97858897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36893363-G-A

97858897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36893363-G-T

http://identifiers.org/hco/2/GRCh38#97858915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36893381-C-A

97859142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36893766-T-C

http://identifiers.org/hco/2/GRCh38#97859180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36893804-C-A

97859319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 36893940-T-C

97859475-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36894106-G-C

97859475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36894106-G-T

97859489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36894120-G-A

97859489-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36894120-G-C

97859489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36894120-G-T

97859509-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36894143-T-G

97859534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36894168-T-C

97859534-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36894168-T-G

http://identifiers.org/hco/2/GRCh38#97860327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36894940-C-A

97860448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36895024-C-T

97860611-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36895164-T-A

97869259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36898670-G-T

http://identifiers.org/hco/2/GRCh38#97869343-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36898744-A-C

97869368-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36898756-T-A

97869385-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36898759-T-A

97869389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36898763-C-T

97869508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36898855-G-A

97869863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36899043-C-T

97870423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36899535-C-T

http://identifiers.org/hco/2/GRCh38#97870494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36899606-C-A

http://identifiers.org/hco/2/GRCh38#97870495-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36899607-A-C

97870785-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 36899872-C-G

http://identifiers.org/hco/2/GRCh38#97870816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36899902-C-A

97870816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36899902-C-T

97870951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36900007-G-A

97871186-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36900158-C-G

97881518-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36904159-T-G

97881695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36904327-G-T

97881727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36904376-G-A

97881727-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36904376-G-C

97882381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36906986-T-C

97882389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36906994-A-G

97882403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36907008-T-C

97882578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36907095-G-A

97882659-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36907149-G-C

97882677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36907167-C-T

97882743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36907232-T-C

97882840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36907337-G-A

97882999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36907513-G-A

97882999-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36907513-G-C

97883079-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36907578-G-C

97883282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36907773-A-G

97883306-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36907797-G-C

97883446-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36907920-T-A

97883446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36907920-T-C

97883484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36907958-T-C

97883484-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36907958-T-G

97883846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36908300-T-C

97883882-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36908338-G-C

97887593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36911197-G-T

97887852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36911439-A-G

97887852-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36911439-A-T

97887995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36911560-T-C

97888154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36911694-T-C

97888257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36911789-G-A

97888293-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36911825-T-G

97888548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36912720-C-T

97888812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36912931-A-G

97889052-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36913125-T-G

97890174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36914331-C-T

97890185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36914344-T-C

http://identifiers.org/hco/2/GRCh38#97890210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36914369-C-A

97890669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36914725-A-G

http://identifiers.org/hco/2/GRCh38#97890756-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36914800-A-C

97890894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36914932-T-C

97891011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36915035-G-A

http://identifiers.org/hco/2/GRCh38#97891014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36915037-C-A

97891014-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36915037-C-G

97891014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36915037-C-T

http://identifiers.org/hco/2/GRCh38#97891146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36915179-C-A

97891352-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36915459-G-C

97891370-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36915478-C-G

97891748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36916037-A-G

97891959-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36916376-G-C

97892021-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36916425-A-T

97892227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36916633-T-C

97907051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36919631-T-C

97908650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 36920407-A-G

97908848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36920604-A-G

97908898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36920679-C-T

97909011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36920791-A-G

97909076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36920852-G-T

http://identifiers.org/hco/2/GRCh38#97909085-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36920861-A-C

97909085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36920861-A-G

http://identifiers.org/hco/2/GRCh38#97909188-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36920939-A-C

97909330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36921045-G-A

97909333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36921048-G-A

97909409-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36921093-T-A

97911804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36922728-G-T

97911856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36922763-T-C

97912134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36922985-T-C

http://identifiers.org/hco/2/GRCh38#97912255-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36923093-A-C

97912725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36923585-T-C

97927221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36928182-T-C

97927598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36928606-T-C

http://identifiers.org/hco/2/GRCh38#97927629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36928636-C-A

http://identifiers.org/hco/2/GRCh38#97929378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36929964-C-A

97929378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36929964-C-T

http://identifiers.org/hco/2/GRCh38#97929912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36930453-C-A

97932270-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36932587-T-A

97932270-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36932587-T-G

97957496-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36950583-T-A

97962605-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36951981-A-T

97962816-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36952191-A-T

97962824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36952210-T-C

97963101-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36952452-T-A

97963113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36952464-T-C

97963140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36952489-G-T

97963371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36952927-T-C

97964018-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36953487-T-A

97964167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36953630-A-G

97964265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36953691-T-C

97964416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36953842-C-T

97964736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36954127-G-A

97966082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36955798-T-C

97966088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36955804-G-A

97966178-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36955851-G-T

97966236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36955903-G-A

97966258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36955924-G-A

97966386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36956277-C-T

http://identifiers.org/hco/2/GRCh38#97966921-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#36956767-A-C

97966929-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36956775-A-T

97966973-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36956816-T-A

97967079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36956888-C-T

97967741-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36957638-G-C

97968348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36958759-A-G

97968381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36958801-A-G

97968678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36959069-G-A

97969420-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36959448-G-C

97969423-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36959451-T-G

97969791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36959797-A-G

97970410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36960395-G-A

97970520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36960501-A-G

97970660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36960643-T-C

97970931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36960909-T-C

97970955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36960953-T-C

97970967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36960965-G-T

97971058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36961050-T-C

97971068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36961060-A-G

97971068-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36961060-A-T

97971070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36961062-A-G

97971160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36961191-C-T

97971410-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36961418-A-T

97971462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36961457-C-T

97984245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36965618-C-T

97984370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36965734-T-C

97984805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36965914-G-A

97985028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36966124-C-T

97985370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36966455-C-T

97985965-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36966593-T-A

97986319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36966935-T-C

97986682-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36968708-C-G

97987012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36969015-G-A

97987023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36969025-A-G

97989735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36971905-G-A

97990506-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36973153-C-G

97991198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36973681-A-G

http://identifiers.org/hco/2/GRCh38#97991328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36973773-C-A

97991495-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36973946-T-A

97991694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36974145-G-A

97992103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36974538-G-T

97992464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36974843-G-A

97993000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36975861-G-A

97993000-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36975861-G-C

97993235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36976078-A-G

97993350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36976220-T-C

97993622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36976516-T-C

97994055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36976892-C-T

97994072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36976909-T-C

97994184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36977012-C-T

97994200-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36977028-G-C

97994679-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36977403-G-C

97994706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36977432-T-C

97994920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36977650-G-A

97995340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 36978149-G-A

97995340-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 36978149-G-T

http://identifiers.org/hco/2/GRCh38#97995420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36978215-C-A

97995420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 36978215-C-T

http://identifiers.org/hco/2/GRCh38#97995422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: http://identifiers.org/mco/1/GRCm39#36978217-C-A

97995422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 36978217-C-T

97995561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: synonymous variant
orthologous variants: 36978331-G-A

97995561-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: synonymous variant
orthologous variants: 36978331-G-C

97995561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: synonymous variant
orthologous variants: 36978331-G-T

97995607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: missense variant
orthologous variants: 36978377-G-A

97995607-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: missense variant
orthologous variants: 36978377-G-C

97995607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: missense variant
orthologous variants: 36978377-G-T

http://identifiers.org/hco/2/GRCh38#97995614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36978384-C-A

97995614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: missense variant
orthologous variants: 36978384-C-T

97995636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: synonymous variant
orthologous variants: 36978400-T-C

97995636-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: synonymous variant
orthologous variants: 36978400-T-G

http://identifiers.org/hco/2/GRCh38#97995725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36978492-C-A

97995725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: 5 prime UTR variant
orthologous variants: 36978492-C-T

97995776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: 5 prime UTR variant
orthologous variants: 36978543-G-A

97995776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: 5 prime UTR variant
orthologous variants: 36978543-G-T

http://identifiers.org/hco/2/GRCh38#97995794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36978561-C-A

97995794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: 5 prime UTR variant
orthologous variants: 36978561-C-T

97995838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: 5 prime UTR variant
orthologous variants: 36978605-G-A

97995838-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: 5 prime UTR variant
orthologous variants: 36978605-G-C

97995838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: 5 prime UTR variant
orthologous variants: 36978605-G-T

97995853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: 5 prime UTR variant
orthologous variants: 36978620-T-C

97995857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: 5 prime UTR variant
orthologous variants: 36978624-T-C

http://identifiers.org/hco/2/GRCh38#97995944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36978711-C-A

97995944-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: 5 prime UTR variant
orthologous variants: 36978711-C-G

97995944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30366
most severe consequence: 5 prime UTR variant
orthologous variants: 36978711-C-T