96875939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: 3 prime UTR variant
orthologous variants: 36601834-A-G

http://identifiers.org/hco/2/GRCh38#96875947-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36601842-A-C

96875947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: 3 prime UTR variant
orthologous variants: 36601842-A-G

96875983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: 3 prime UTR variant
orthologous variants: 36601880-A-G

http://identifiers.org/hco/2/GRCh38#96875985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36601882-C-A

96875985-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: 3 prime UTR variant
orthologous variants: 36601882-C-G

96875985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: 3 prime UTR variant
orthologous variants: 36601882-C-T

96875996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: 3 prime UTR variant
orthologous variants: 36601893-G-A

96875996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: 3 prime UTR variant
orthologous variants: 36601893-G-T

96876029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36601908-G-A

96876029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36601908-G-T

96876214-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36602020-T-A

96876214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36602020-T-C

96876338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36602130-G-A

96876338-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36602130-G-C

96876388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36602184-T-C

96876422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36602198-G-A

96876422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36602198-G-T

96876472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36602241-G-A

http://identifiers.org/hco/2/GRCh38#96876657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36602433-C-A

96876981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36602687-C-T

96877147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36602851-T-C

96877821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36603336-G-A

96877821-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36603336-G-C

96877839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36603354-G-A

96877839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36603354-G-T

96878040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 36603561-G-A

96878040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 36603561-G-T

96878104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36603623-G-T

96878253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36603743-G-A

96878329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36603815-G-A

96878329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36603815-G-T

96878342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36603828-G-A

96878342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36603828-G-T

http://identifiers.org/hco/2/GRCh38#96878536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36604017-C-A

96878536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36604017-C-T

96878570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36604043-C-T

http://identifiers.org/hco/2/GRCh38#96878579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36604049-C-A

96878579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36604049-C-T

96878854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36604290-T-C

96878857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36604293-G-A

96878862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36604298-C-T

96878864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36604300-G-T

96878960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36604502-G-A

96878980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36604522-C-T

96879341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36605078-T-C

http://identifiers.org/hco/2/GRCh38#96879489-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36605188-A-C

96879549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36605237-G-A

96879835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36605467-G-A

96880065-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36605557-G-C

96880100-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36605575-G-C

http://identifiers.org/hco/2/GRCh38#96880146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36605619-C-A

96880194-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36605660-G-C

96880268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36605733-G-A

96880480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36606003-G-A

96880497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36606022-G-A

96881380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-T

96881381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

96881585-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: -T-G

96881611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-T

96881635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

96881878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

96882677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36608666-G-A

http://identifiers.org/hco/2/GRCh38#96882924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36608925-C-A

96882924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36608925-C-T

96883358-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36609320-C-G

96883439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36609391-A-G

http://identifiers.org/hco/2/GRCh38#96883805-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36609683-A-C

96883967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36609880-G-A

96883967-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36609880-G-C

96883980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36609893-G-A

http://identifiers.org/hco/2/GRCh38#96884385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#36610287-C-A

96884819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36610659-G-A

96884856-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36610696-G-C

96884883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36610723-C-T

96884903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36610743-G-A

96885264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36611099-G-A

96885809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36611608-T-C

96885964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36611744-C-T

96886175-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36611844-G-C

96886259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36611928-C-T

96886272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36611941-C-T

96886430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36612019-G-A

96886434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36612023-G-T

96888048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36612903-C-T

96888065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36612920-T-C

96888512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36613318-C-T

http://identifiers.org/hco/2/GRCh38#96888779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#36613579-C-A

96888779-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36613579-C-G

96888779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36613579-C-T

96888889-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36613659-C-G

96888889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36613659-C-T

96888949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36613740-T-C

96888949-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36613740-T-G

96888963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36613754-G-A

http://identifiers.org/hco/2/GRCh38#96888964-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36613755-A-C

96889076-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36613823-T-A

96889226-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36613964-T-A

96889227-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36613965-C-G

96889286-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36614046-C-G

96890652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36614578-T-C

96890849-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36614761-T-G

96891016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36615036-C-T

http://identifiers.org/hco/2/GRCh38#96891597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36615573-C-A

96891644-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36615589-A-T

http://identifiers.org/hco/2/GRCh38#96891819-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36615765-A-C

96891911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36615842-G-A

96892054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36615982-G-A

96892057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36615985-G-A

96892123-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36616050-T-A

96892123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36616050-T-C

96892132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36616059-A-G

http://identifiers.org/hco/2/GRCh38#96892274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36616186-C-A

96892480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36616399-G-A

96892930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36616799-G-T

http://identifiers.org/hco/2/GRCh38#96892977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36616845-C-A

96893004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36616879-C-T

96893166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36617043-C-T

96893180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36617057-A-G

96893189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36617066-T-C

96893317-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36617158-T-G

96893720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36617389-C-T

96893725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36617395-C-T

96893824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36617502-G-A

96893824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36617502-G-T

http://identifiers.org/hco/2/GRCh38#96893860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36617538-C-A

96893860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36617538-C-T

http://identifiers.org/hco/2/GRCh38#96893889-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36617566-C-A

96893889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36617566-C-T

96893895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36617572-G-A

96893909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36617586-G-A

96893944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36617618-A-G

96894057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 36617731-G-A

http://identifiers.org/hco/2/GRCh38#96894173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36617825-C-A

96894238-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36617888-G-C

96894298-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36617956-C-G

http://identifiers.org/hco/2/GRCh38#96894300-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36617958-A-C

http://identifiers.org/hco/2/GRCh38#96894302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36617960-C-A

96894302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36617960-C-T

http://identifiers.org/hco/2/GRCh38#96894304-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36617962-A-C

96895408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36618913-G-A

96895595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, undefined
orthologous variants: 36619055-T-C

96895654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, undefined
orthologous variants: 36619121-C-T

96895974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36619446-G-A

96895974-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36619446-G-C

96896388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36619835-G-A

96898703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36622214-T-C

96898724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36622249-G-A

96898724-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36622249-G-C

96898828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36622335-G-A

96898858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36622359-G-T

http://identifiers.org/hco/2/GRCh38#96899007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36622446-C-A

96899007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36622446-C-T

96902451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36624822-C-T

96902481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36624849-G-A

96902481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36624849-G-T

96902512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36624875-A-G

96902512-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36624875-A-T

96902560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36624943-G-T

96902719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36625099-G-A

96902719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36625099-G-T

96902743-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36625122-T-A

96902743-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36625122-T-G

http://identifiers.org/hco/2/GRCh38#96903611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#36625782-C-A

96903611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, undefined
orthologous variants: 36625782-C-T

96903716-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36625881-G-C

96903959-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36626758-C-G

http://identifiers.org/hco/2/GRCh38#96906523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36627404-C-A

96906583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36627466-G-A

96906656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36627538-C-T

96906924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36627777-G-A

96906924-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36627777-G-C

96906925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36627778-C-T

http://identifiers.org/hco/2/GRCh38#96906995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36627849-C-A

96907092-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36627993-G-C

96907249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36628128-G-A

96907306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36628173-T-C

96907362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36628236-G-A

96907677-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36628543-C-G

96907763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36628639-G-A

96907792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36628668-T-C

96907800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36628678-C-T

96908062-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36628925-T-G

96908257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36629177-T-C

96908299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36629208-C-T

96909337-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36629679-T-G

96909451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36629780-T-C

96909573-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36629897-C-G

96909583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36629907-G-A

96909610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36629942-C-T

96909918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36630235-G-T

96910008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36630267-G-A

96910195-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36630399-C-G

96910222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36630412-A-G

96910441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36630640-T-C

96910483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36630684-G-A

96910508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36630689-C-T

96910509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36630690-G-A

http://identifiers.org/hco/2/GRCh38#96910881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36630912-C-A

96911278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36631162-G-A

http://identifiers.org/hco/2/GRCh38#96911287-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36631171-A-C

96911450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36631307-G-A

96913251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36631951-G-A

96916235-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36634563-A-T

96916486-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36634789-T-A

96916558-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36634889-C-G

96916777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36635261-C-T

96916953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36635440-C-T

96916958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36635445-C-T

96916977-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36635462-G-C

96917300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36636872-C-T

96917362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36636929-C-T

96917489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36637035-G-A

96917510-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36637056-A-T

96920666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36638741-C-T

http://identifiers.org/hco/2/GRCh38#96920870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36638915-C-A

96920870-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36638915-C-G

96920870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36638915-C-T

96921088-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36639149-G-C

96921088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36639149-G-T

96921200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 36639239-G-A

96921200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 36639239-G-T

96921242-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 36639281-G-C

http://identifiers.org/hco/2/GRCh38#96921302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36639341-C-A

96921302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36639341-C-T

http://identifiers.org/hco/2/GRCh38#96921326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36639357-C-A

http://identifiers.org/hco/2/GRCh38#96921556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36639567-C-A

http://identifiers.org/hco/2/GRCh38#96921623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36639634-C-A

96921623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36639634-C-T

96921647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36639658-G-A

96921647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36639658-G-T

96923379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36639847-A-G

96923451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36639912-G-T

96923538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 36639996-G-A

96923538-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36639996-G-C

96923593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36640042-G-A

96923593-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36640042-G-C

http://identifiers.org/hco/2/GRCh38#96923706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36640184-C-A

96923717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36640235-A-G

96923970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36640608-G-T

96924115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36640714-G-A

96924115-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36640714-G-C

96924187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36640781-G-A

96924226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36640820-G-A

http://identifiers.org/hco/2/GRCh38#96924757-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36642212-A-C

96924836-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36642302-T-G

96924963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36642418-G-A

96925064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36642513-T-C

96925191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36642645-G-A

96925700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36643205-G-A

96925701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36643206-G-A

96926603-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36644369-C-G

http://identifiers.org/hco/2/GRCh38#96926706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36644438-C-A

96927418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36645750-G-A

96927555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36645856-C-T

http://identifiers.org/hco/2/GRCh38#96927595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36645893-C-A

96927595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36645893-C-T

96928413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36646503-C-T

96929186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36647479-G-A

96929186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36647479-G-T

96929211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36647503-A-G

96929362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36647651-G-A

96929362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36647651-G-T

http://identifiers.org/hco/2/GRCh38#96929389-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36647675-A-C

96929389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36647675-A-G

96929392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36647678-G-A

96929392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36647678-G-T

96929549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36647807-G-T

96929740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36647958-C-T

96929841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36648054-T-C

96931797-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36650524-T-A

96932043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36650746-G-A

96932469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36651115-C-T

96933309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36651270-G-A

96933484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36651462-C-T

96933810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36651703-G-A

96933819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36651712-C-T

96934032-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36651862-A-T

96934264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36652087-T-C

96934538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36652335-C-T

96934580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36652420-A-G

96934621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36652460-G-A

96938001-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36659682-T-A

96938347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36660000-G-A

96938479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36660137-T-C

96938663-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36660302-C-G

96938965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36660760-G-A

96938965-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36660760-G-T

http://identifiers.org/hco/2/GRCh38#96939093-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36660858-C-A

96939093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36660858-C-T

96939128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36660874-G-A

96941626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36664458-C-T

96944973-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36669299-T-G

96945403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36669627-T-C

http://identifiers.org/hco/2/GRCh38#96945598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36669755-C-A

96946062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36670073-C-T

96946172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36670146-C-T

96946278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36670228-G-A

96946278-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36670228-G-C

http://identifiers.org/hco/2/GRCh38#96946767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36670614-C-A

96947028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36670862-C-T

96947402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36671146-T-C

96947402-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36671146-T-G

96947579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36671304-C-T

http://identifiers.org/hco/2/GRCh38#96947733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36671454-C-A

96947733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36671454-C-T

http://identifiers.org/hco/2/GRCh38#96947736-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36671457-C-A

96947736-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36671457-C-G

http://identifiers.org/hco/2/GRCh38#96950008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36672965-C-A

96950008-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36672965-C-G

96950008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36672965-C-T

http://identifiers.org/hco/2/GRCh38#96950015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36672972-C-A

96950015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36672972-C-T

96950028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36672985-G-A

96950028-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36672985-G-C

96950028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36672985-G-T

http://identifiers.org/hco/2/GRCh38#96950043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36673000-C-A

96950043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36673000-C-T

96950253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36673212-C-T

96950744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36673661-T-C

96950985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36673873-C-T

96951005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36673893-T-C

http://identifiers.org/hco/2/GRCh38#96951113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36673999-C-A

96951113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36673999-C-T

96951144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36674033-G-A

http://identifiers.org/hco/2/GRCh38#96951249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#36674129-C-A

96951249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36674129-C-T

96951293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36674160-G-A

96951293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36674160-G-T

http://identifiers.org/hco/2/GRCh38#96951320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36674188-C-A

96951320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36674188-C-T

http://identifiers.org/hco/2/GRCh38#96951478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#36674347-C-A

96951478-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 36674347-C-G

96951478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 36674347-C-T

96951528-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36674421-C-G

96951528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36674421-C-T

96951542-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36674431-T-A

96951542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36674431-T-C

96951608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36674493-A-G

96951657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36674540-A-G

96952171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36674742-G-A

96952564-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36675079-T-A

96952564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36675079-T-C

96952656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36675140-G-A

96952669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36675153-C-T

96952705-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36675182-T-G

96952729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36675203-C-T

96953211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36675575-T-C

96953340-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36675663-G-C

96954003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36676236-G-A

96954140-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36676627-A-T

96954425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36677141-T-C

96957340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36679353-C-T

96957345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36679358-C-T

96957778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36679831-A-G

96957789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36679842-A-G

96957910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36679945-T-C

96958017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36680047-A-G

96958037-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36680067-G-C

96958055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36680086-G-T

96960398-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: synonymous variant
orthologous variants: 36683401-C-G

96960398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: synonymous variant
orthologous variants: 36683401-C-T

96961592-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36684751-T-A

http://identifiers.org/hco/2/GRCh38#96961689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36684828-C-A

http://identifiers.org/hco/2/GRCh38#96961849-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36684977-A-C

96961849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36684977-A-G

96961929-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36685054-C-G

96961929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36685054-C-T

96962484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36685180-G-A

96962829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36685541-A-G

96962894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36685604-C-T

96962895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36685605-C-T

96963141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36685861-C-T

96963407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36686803-C-T

http://identifiers.org/hco/2/GRCh38#96967451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: -C-A

96967451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: -C-T

96967528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: synonymous variant
orthologous variants: 36695900-G-A

96967528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: synonymous variant
orthologous variants: 36695900-G-T

http://identifiers.org/hco/2/GRCh38#96967540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36695923-C-A

96967540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: synonymous variant
orthologous variants: 36695923-C-T

96967548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: missense variant
orthologous variants: 36695935-C-T

96970433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36698202-G-T

96970434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36698203-G-A

96970557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36698289-C-T

96970568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36698298-A-G

http://identifiers.org/hco/2/GRCh38#96970588-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36698317-A-C

96970588-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36698317-A-T

96970640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36698369-C-T

96970760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: synonymous variant
orthologous variants: 36698489-T-C

96970803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36698532-G-A

96970803-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36698532-G-C

96970803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36698532-G-T

96970832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36698545-G-A

96970832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36698545-G-T

96970871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36698584-T-C

96970871-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36698584-T-G

96970908-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36698615-T-A

96970908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36698615-T-C

96970909-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36698616-T-A

96971373-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36699259-G-C

96971373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36699259-G-T

96971422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36699333-C-T

http://identifiers.org/hco/2/GRCh38#96971668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36699552-C-A

96971772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36699663-G-A

96971772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36699663-G-T

http://identifiers.org/hco/2/GRCh38#96971776-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36699667-A-C

96971776-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36699667-A-T

96971874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36699786-A-G

96971935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: missense variant
orthologous variants: 36699850-G-A

96971935-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: missense variant
orthologous variants: 36699850-G-C

96971935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: missense variant
orthologous variants: 36699850-G-T

96972192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: synonymous variant
orthologous variants: 36700050-G-A

http://identifiers.org/hco/2/GRCh38#96972252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36700098-C-A

96972252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: synonymous variant
orthologous variants: 36700098-C-T

http://identifiers.org/hco/2/GRCh38#96972267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36700113-C-A

96972267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: synonymous variant
orthologous variants: 36700113-C-T

96972438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36700255-T-C

http://identifiers.org/hco/2/GRCh38#96972745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36700541-C-A

http://identifiers.org/hco/2/GRCh38#96972746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36700542-C-A

96972746-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36700542-C-G

96973066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36700753-G-A

96973070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36700757-G-A

96973140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36700818-A-G

http://identifiers.org/hco/2/GRCh38#96973149-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36700827-A-C

http://identifiers.org/hco/2/GRCh38#96973511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36701117-C-A

96973557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36701163-A-G

http://identifiers.org/hco/2/GRCh38#96973655-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36701281-A-C

http://identifiers.org/hco/2/GRCh38#96977436-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: -A-C

96977436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: -A-G

96977683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: -G-A

96977683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: -G-T

96977715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: -A-G

http://identifiers.org/hco/2/GRCh38#96977837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: -C-A

96977837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: -C-T

http://identifiers.org/hco/2/GRCh38#96977992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: -C-A

96977992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: -C-T

http://identifiers.org/hco/2/GRCh38#96978143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: -C-A

96978143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: -C-T

96978226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: -T-C

96985455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36721169-G-A

96985455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36721169-G-T

96985612-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36721341-C-G

96985649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36721378-A-G

96985690-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36721419-C-G

96985818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36721537-C-T

96986071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36721837-G-A

96986071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36721837-G-T

96986075-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36721841-C-G

96986075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36721841-C-T

96986090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36721850-G-T

http://identifiers.org/hco/2/GRCh38#96986132-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36721883-A-C

96986150-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36721900-G-C

96986150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: intron variant
orthologous variants: 36721900-G-T

http://identifiers.org/hco/2/GRCh38#96986295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36722002-C-A

96986295-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: missense variant
orthologous variants: 36722002-C-G

96986295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: missense variant
orthologous variants: 36722002-C-T

96986305-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: synonymous variant
orthologous variants: 36722012-T-A

96986305-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: synonymous variant
orthologous variants: 36722012-T-G

http://identifiers.org/hco/2/GRCh38#96986480-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28036
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36722158-A-C