233776675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88151275-G-A

233776719-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88151321-C-G

233776796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88151396-A-G

http://identifiers.org/hco/2/GRCh38#233776888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88151465-C-A

233777111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88151657-A-G

233777400-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88151929-G-C

233777847-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88154290-T-A

233777918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88154355-T-C

233777966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88154440-C-T

233777985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88154459-C-T

233778052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88154522-G-T

233778160-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88154620-G-T

233778185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88154645-G-A

233778185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88154645-G-T

http://identifiers.org/hco/2/GRCh38#233778203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88154661-C-A

233778213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88154671-T-C

233778219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 88154673-A-G

233778278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 88154732-G-T

http://identifiers.org/hco/2/GRCh38#233778436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88154893-C-A

233778492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88154949-A-G

233778639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88155054-T-C

http://identifiers.org/hco/2/GRCh38#233778910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88155304-C-A

233778940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88155357-G-A

233778986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88155401-A-G

233779011-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88155426-T-A

233779046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88155460-C-T

233779143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88155551-C-T

233779203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88155639-A-G

http://identifiers.org/hco/2/GRCh38#233779208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88155644-C-A

233779221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88155657-G-T

233779253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88155684-G-A

233779253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88155684-G-T

233779260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88155691-G-A

233779260-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88155691-G-C

233779273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88155703-G-A

233779273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88155703-G-T

http://identifiers.org/hco/2/GRCh38#233779290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88155722-C-A

233779291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88155723-A-G

233779407-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant
orthologous variants: 88155823-T-G

233779424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 88155840-C-T

http://identifiers.org/hco/2/GRCh38#233779556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88155888-C-A

233779556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88155888-C-T

233779560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88155892-A-G

233779560-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88155892-A-T

233779720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88155998-A-G

233779777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88156055-G-A

233779787-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88156065-G-C

233779813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88156091-A-G

233779823-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88156101-A-T

233779930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88156220-G-A

233779930-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88156220-G-C

233779930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88156220-G-T

http://identifiers.org/hco/2/GRCh38#233779936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88156225-C-A

233779946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88156235-A-G

233779947-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88156236-T-G

233780020-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88156308-A-T

233788819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88157426-G-A

233788869-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88157467-G-C

233788907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88157483-C-T

233788928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88157497-G-T

233789047-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88157690-G-C

233789204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88157796-A-G

http://identifiers.org/hco/2/GRCh38#233789376-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88157945-A-C

233789376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88157945-A-G

233789412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88157976-A-G

233789423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88157987-A-G

233789441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88158005-G-A

233789441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88158005-G-T

233789442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88158008-G-A

233789442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88158008-G-T

http://identifiers.org/hco/2/GRCh38#233789475-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88158043-A-C

233789475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88158043-A-G

http://identifiers.org/hco/2/GRCh38#233789502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88158069-C-A

233789502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 88158069-C-T

http://identifiers.org/hco/2/GRCh38#233789509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88158076-C-A

233789509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 88158076-C-T

233789515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 88158082-G-A

233789515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 88158082-G-T

233789523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 88158090-T-C

233789586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 88158153-G-A

233789586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 88158153-G-T

http://identifiers.org/hco/2/GRCh38#233789595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88158162-C-A

233789595-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 88158162-C-G

233789595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 88158162-C-T

233789643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88158212-T-C

http://identifiers.org/hco/2/GRCh38#233789657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88158225-C-A

233789657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88158225-C-T

233789663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88158231-G-A

233789750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88158298-G-T

233789816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88158324-T-C

233789854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 88158350-G-T

233789863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 88158359-T-C

233789870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 88158366-G-A

233789870-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 88158366-G-C

233789876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 88158372-G-A

233789876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 88158372-G-T

233789879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 88158375-G-A

233789879-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 88158375-G-T

233789893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 88158389-G-A

233789893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 88158389-G-T

233789894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 88158390-G-T

http://identifiers.org/hco/2/GRCh38#233789906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88158402-C-A

233789906-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 88158402-C-G

233789906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 88158402-C-T

233789972-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 88158468-G-C

233790050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88158543-G-A

233790050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88158543-G-T

http://identifiers.org/hco/2/GRCh38#233790066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88158558-C-A

233790066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88158558-C-T

http://identifiers.org/hco/2/GRCh38#233790071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88158563-C-A

233790072-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88158564-T-A

233790072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88158564-T-C

233790093-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88158577-T-A

233790093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88158577-T-C

233790111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88158595-T-C

http://identifiers.org/hco/2/GRCh38#233790119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88158610-C-A

233790119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88158610-C-T

233790127-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88158618-T-A

233790127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88158618-T-C

http://identifiers.org/hco/2/GRCh38#233790141-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88158654-A-C

233790141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88158654-A-G

233790141-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88158654-A-T

233790169-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88158682-T-A

233790267-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88158766-C-G

233792719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88159892-G-A

233792719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88159892-G-T

233792819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 88159989-G-T

http://identifiers.org/hco/2/GRCh38#233792876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88160046-C-A

233792876-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 88160046-C-G

233792876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 88160046-C-T

http://identifiers.org/hco/2/GRCh38#233792940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88160111-C-A

233792940-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88160111-C-G

233792940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88160111-C-T

233792959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88160121-A-G

233792979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88160141-G-A

233792979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88160141-G-T

http://identifiers.org/hco/2/GRCh38#233793001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88160156-C-A

http://identifiers.org/hco/2/GRCh38#233793030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88160187-C-A

233793030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88160187-C-T

233793080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88160473-G-A

233793110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88160576-G-A

233793110-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88160576-G-C

233793122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88160605-G-A

233793183-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88160650-C-G

233793213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88160680-G-A

233793221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88160688-G-A

233793221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88160688-G-T

233793239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88160705-T-C

233793278-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88160745-C-G

233793561-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88160971-T-A

233793561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88160971-T-C

233793561-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88160971-T-G

http://identifiers.org/hco/2/GRCh38#233793567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88160977-C-A

233793567-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88160977-C-G

233793571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88160981-G-A

233793571-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88160981-G-C

233793571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88160981-G-T

233793616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88161002-T-C

233793628-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88161008-C-G

233793628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88161008-C-T

233793659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88161025-G-A

233793669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 88161035-G-A

233793670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 88161036-T-C

http://identifiers.org/hco/2/GRCh38#233793683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88161049-C-A

http://identifiers.org/hco/2/GRCh38#233793686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88161052-C-A

http://identifiers.org/hco/2/GRCh38#233793694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88161060-C-A

233793694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88161060-C-T

233793695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88161061-G-A

233793695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88161061-G-T

233793696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88161062-G-A

233793696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88161062-G-T

233793746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88161112-T-C

233793747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88161113-G-A

233793749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88161115-G-T

http://identifiers.org/hco/2/GRCh38#233793773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88161139-C-A

233793773-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88161139-C-G

233793773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88161139-C-T

http://identifiers.org/hco/2/GRCh38#233793783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88161149-C-A

233793783-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88161149-C-G

233793783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88161149-C-T

233793784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88161150-G-A

233793784-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88161150-G-C

233793784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88161150-G-T

http://identifiers.org/hco/2/GRCh38#233793791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88161157-C-A

233793791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88161157-C-T

233793798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88161164-G-A

http://identifiers.org/hco/2/GRCh38#233793804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88161170-C-A

233793804-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88161170-C-G

233793804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88161170-C-T

http://identifiers.org/hco/2/GRCh38#233793835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88161201-C-A

233793835-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88161201-C-G

233793835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88161201-C-T

http://identifiers.org/hco/2/GRCh38#233793836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88161202-C-A

233793836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88161202-C-T

233793844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88161209-G-A

233793844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88161209-G-T

233793848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88161213-G-A

233793848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88161213-G-T

233793897-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 88161248-T-G

http://identifiers.org/hco/2/GRCh38#233793911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88161262-C-A

233793911-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 88161262-C-G

233793911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 88161262-C-T

233793918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 88161269-A-G

http://identifiers.org/hco/2/GRCh38#233793919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88161270-C-A

233793919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 88161270-C-T

233793924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant
orthologous variants: 88161275-A-G

233794059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88161397-T-C

http://identifiers.org/hco/2/GRCh38#233794222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88161582-C-A

233794222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88161582-C-T

233794234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88161616-G-A

233794234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88161616-G-T

http://identifiers.org/hco/2/GRCh38#233794240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88161622-C-A

233794240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88161622-C-T

233794284-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88161666-T-A

233794284-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88161666-T-G

233794296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88161675-G-A

233794296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88161675-G-T

233794335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88161711-G-T

http://identifiers.org/hco/2/GRCh38#233794401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88161762-C-A

233794401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 88161762-C-T

233794422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 88161783-T-C

http://identifiers.org/hco/2/GRCh38#233794497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88161858-C-A

233794497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 88161858-C-T

233794498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant
orthologous variants: 88161859-G-A

233794498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant
orthologous variants: 88161859-G-T

http://identifiers.org/hco/2/GRCh38#233794627-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88161991-A-C

233795287-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88162316-G-C

233795477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88162511-G-A

233795477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88162511-G-T

http://identifiers.org/hco/2/GRCh38#233795531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88162562-C-A

233795531-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88162562-C-G

233795531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88162562-C-T

http://identifiers.org/hco/2/GRCh38#233795543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88162593-C-A

233795543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88162593-C-T

http://identifiers.org/hco/2/GRCh38#233795576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88162622-C-A

233795576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88162622-C-T

233795577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88162623-C-T

233795578-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88162624-C-G

http://identifiers.org/hco/2/GRCh38#233795581-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88162627-A-C

233795582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88162628-G-A

233795582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88162628-G-T

233795584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88162630-A-G

http://identifiers.org/hco/2/GRCh38#233795679-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88162718-A-C

233795679-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: synonymous variant
orthologous variants: 88162718-A-T

233795736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: synonymous variant
orthologous variants: 88162775-G-A

233795739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: synonymous variant
orthologous variants: 88162778-C-T

233795740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense variant
orthologous variants: 88162779-G-A

233795773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88162799-G-A

233795775-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88162801-G-C

233795775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88162801-G-T

233795795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88162820-C-T

233795810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88162836-G-A

233795835-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88162848-C-G

233795835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88162848-C-T

233795857-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88162870-A-T

http://identifiers.org/hco/2/GRCh38#233795879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88162873-C-A

http://identifiers.org/hco/2/GRCh38#233795961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88162906-C-A

233795961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 88162906-C-T

233795988-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense variant
orthologous variants: 88162933-C-G

233795988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: stop gained
orthologous variants: 88162933-C-T

233795993-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense variant
orthologous variants: 88162938-T-A

233795993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: synonymous variant
orthologous variants: 88162938-T-C

233796007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense variant
orthologous variants: 88162952-A-G

233796012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: synonymous variant
orthologous variants: 88162957-C-T

233796017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense variant
orthologous variants: 88162962-G-A

233796023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense variant
orthologous variants: 88162968-G-A

233796031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense variant
orthologous variants: 88162976-G-A

233796031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense variant
orthologous variants: 88162976-G-T

233796092-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88163003-G-C

233796103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88163012-G-A

233796112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88163021-G-A

233796112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88163021-G-T

233796163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88163055-C-T

233796164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88163056-G-A

233796164-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88163056-G-C

233796164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88163056-G-T

233796183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88163078-G-A

http://identifiers.org/hco/2/GRCh38#233796202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88163097-C-A

233796202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 88163097-C-T

233796203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense variant
orthologous variants: 88163098-G-A

http://identifiers.org/hco/2/GRCh38#233796212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88163107-C-A

233796212-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense variant
orthologous variants: 88163107-C-G

233796212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense variant
orthologous variants: 88163107-C-T

233796269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense variant
orthologous variants: 88163164-G-A

233796269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense variant
orthologous variants: 88163164-G-T

233796274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense variant
orthologous variants: 88163169-G-A

233796274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense variant
orthologous variants: 88163169-G-T

233796276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: synonymous variant
orthologous variants: 88163171-G-T

233796307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88163202-G-A

233796318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88163213-G-A

233796397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88163261-T-C

233796441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88163298-G-T

233796451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88163308-T-C

233796529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88163382-G-A

233796534-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88163392-G-T

http://identifiers.org/hco/2/GRCh38#233798631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88164243-C-A

233798631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88164243-C-T

http://identifiers.org/hco/2/GRCh38#233798645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88164256-C-A

233798645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88164256-C-T

233798670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88164281-G-A

233798670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88164281-G-T

233798673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88164284-G-A

233798673-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88164284-G-C

233798673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88164284-G-T

233798692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88164303-A-G

233798692-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88164303-A-T

http://identifiers.org/hco/2/GRCh38#233798725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88164332-C-A

233798746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88164353-T-C

233798784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88164387-G-A

233798784-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88164387-G-C

233798786-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88164389-G-C

233798814-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88164417-G-C

233798814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88164417-G-T

233798817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88164420-A-G

http://identifiers.org/hco/2/GRCh38#233798898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88164475-C-A

http://identifiers.org/hco/2/GRCh38#233798899-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88164476-A-C

233798993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88164534-G-A

233798994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88164535-A-G

233798996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88164537-G-T

233799015-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88164556-C-G

233799016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88164557-C-T

233799086-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88164609-C-G

233799158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88164655-C-T

233799188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88164688-C-T

233799218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88164718-A-G

233799359-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88164799-G-C

233799415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88164835-G-A

233799415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88164835-G-T

233799422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88164842-G-A

233799427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88164847-G-A

233799427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88164847-G-T

233799438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88164858-C-T

233799446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88164866-T-C

233799508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88164921-G-A

233799584-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88164985-G-C

http://identifiers.org/hco/2/GRCh38#233799614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88165015-C-A

233799621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88165022-A-G

233799640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88165041-A-G

233799640-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88165041-A-T

233799701-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88165102-C-G

http://identifiers.org/hco/2/GRCh38#233799748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88165164-C-A

233799748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88165164-C-T

233799764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88165179-G-A

233799764-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88165179-G-C

233799764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88165179-G-T

http://identifiers.org/hco/2/GRCh38#233799893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/1/GRCm39#88165308-C-A

233799914-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88165329-T-A

http://identifiers.org/hco/2/GRCh38#233799925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88165340-C-A

233799972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88165385-T-C

http://identifiers.org/hco/2/GRCh38#233800044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88165436-C-A

233800044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88165436-C-T

233800046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88165438-G-T

233800087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88165456-G-A

233800087-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88165456-G-C

233800087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88165456-G-T

233800103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88165471-G-A

233800103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88165471-G-T

233800104-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88165472-T-A

233800132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88165501-A-G

233800133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88165502-G-A

233800136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88165505-G-A

233800136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88165505-G-T

233800142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88165511-A-G

233800142-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88165511-A-T

http://identifiers.org/hco/2/GRCh38#233800153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88165522-C-A

233800153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88165522-C-T

http://identifiers.org/hco/2/GRCh38#233800166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88165535-C-A

233800166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88165535-C-T

233800167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88165536-T-C

233800167-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88165536-T-G

233800190-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88165551-G-C

233800190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88165551-G-T

233800212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88165574-G-A

233800212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88165574-G-T

http://identifiers.org/hco/2/GRCh38#233800213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88165575-C-A

233800213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88165575-C-T

233800303-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88165665-T-A

233800304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88165666-G-A

233800304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88165666-G-T

http://identifiers.org/hco/2/GRCh38#233800336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88165690-C-A

233800336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88165690-C-T

233800344-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88165698-T-A

233800344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88165698-T-C

233801593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88166112-A-G

233801601-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88166120-T-A

233801714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88166219-C-T

233801750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88166254-G-A

233801825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88166329-G-A

233801841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88166345-G-A

233801877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88166379-G-A

233801877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88166379-G-T

http://identifiers.org/hco/2/GRCh38#233802019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88166462-C-A

233802019-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88166462-C-G

233802019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88166462-C-T

233802029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88166472-A-G

233802102-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88166537-T-A

233802102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88166537-T-C

233802103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88166538-G-A

233802103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88166538-G-T

http://identifiers.org/hco/2/GRCh38#233802124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88166573-C-A

233802124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88166573-C-T

233802145-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88166594-T-A

233802145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88166594-T-C

http://identifiers.org/hco/2/GRCh38#233802154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88166602-C-A

233802154-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88166602-C-G

233802154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88166602-C-T

233802163-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 88166611-C-G

233802163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 88166611-C-T

233802247-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88166695-C-G

233802257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88166705-A-G

233802258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88166706-G-A

233802274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88166722-G-A

233802280-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88166728-A-T

233802320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88166768-G-A

233802320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88166768-G-T

233802330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88166778-T-C

233802350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88166799-G-T

233802416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88166856-C-T

233802419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88166859-T-C

http://identifiers.org/hco/2/GRCh38#233802487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88166889-C-A

233802487-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88166889-C-G

233802487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88166889-C-T

http://identifiers.org/hco/2/GRCh38#233802529-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88166932-A-C

http://identifiers.org/hco/2/GRCh38#233802553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88166957-C-A

233802553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88166957-C-T

233802556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88166960-A-G

233802557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88166961-G-T

233802571-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88166975-T-A

233802571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88166975-T-C

233802571-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88166975-T-G

233802588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88166997-G-T

http://identifiers.org/hco/2/GRCh38#233802604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88167013-C-A

233802604-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88167013-C-G

233802604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88167013-C-T

233802721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88167132-G-A

233802744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88167154-C-T

233802755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88167164-T-C

233802767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88167174-A-G

233802799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88167208-G-A

233802956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88167381-T-C

233803097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88167519-G-A

233803100-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88167522-T-A

233803293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88167702-T-C

http://identifiers.org/hco/2/GRCh38#233803307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88167716-C-A

233803307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88167716-C-T

http://identifiers.org/hco/2/GRCh38#233803356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88167755-C-A

233803356-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88167755-C-G

233803392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88167786-G-A

233803392-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88167786-G-C

http://identifiers.org/hco/2/GRCh38#233803399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88167793-C-A

233803399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88167793-C-T

http://identifiers.org/hco/2/GRCh38#233803453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88167846-C-A

http://identifiers.org/hco/2/GRCh38#233803460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88167853-C-A

233803460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense variant
orthologous variants: 88167853-C-T

233803478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense variant
orthologous variants: 88167871-C-T

233803487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 88167880-T-C

233803529-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88167915-C-G

233803529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88167915-C-T

http://identifiers.org/hco/2/GRCh38#233803533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88167919-C-A

233803533-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88167919-C-G

233803544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88167930-C-T

http://identifiers.org/hco/2/GRCh38#233803572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88167958-C-A

233803572-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88167958-C-G

233803574-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88167960-C-G

233803574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88167960-C-T

233803675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88168064-T-C

233803881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88168229-T-C

233803901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88168249-G-A

233803901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88168249-G-T

233803956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88168310-G-A

233804067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense variant
orthologous variants: 88168417-C-T

233804075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense variant
orthologous variants: 88168425-G-A

233804075-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense variant
orthologous variants: 88168425-G-C

233804075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense variant
orthologous variants: 88168425-G-T

233804081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense variant
orthologous variants: 88168431-G-T

http://identifiers.org/hco/2/GRCh38#233804145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88168495-C-A

233804145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense variant
orthologous variants: 88168495-C-T

233804238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88168561-G-A

http://identifiers.org/hco/2/GRCh38#233804260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88168587-C-A

233804260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88168587-C-T

233804300-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88168626-A-T

http://identifiers.org/hco/2/GRCh38#233804301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88168627-C-A

233804345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88168658-G-A

233804345-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88168658-G-C

233804345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88168658-G-T

233804378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88168691-G-A

233804378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88168691-G-T

233804383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88168696-T-C

233804402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88168715-G-A

233804444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88168745-G-A

233804481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88168779-A-G

233804481-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88168779-A-T

233804539-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense variant
orthologous variants: 88168837-C-G

http://identifiers.org/hco/2/GRCh38#233804553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88168851-C-A

233804553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88168851-C-T

233804584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88168881-G-A

233804584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88168881-G-T

233804585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88168882-G-A

http://identifiers.org/hco/2/GRCh38#233804627-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88168919-C-A

233804627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88168919-C-T

233804660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88168945-G-A

233804660-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88168945-G-C

233804671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88168955-G-T

233804812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88169081-G-A

233804813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88169082-C-T

http://identifiers.org/hco/2/GRCh38#233804825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88169094-C-A

233804847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88169113-G-A

233804871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88169140-G-T

233804872-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88169141-A-T

http://identifiers.org/hco/2/GRCh38#233804906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88169167-C-A

233804906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88169167-C-T

233804946-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88169208-G-C

233804946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88169208-G-T

233804970-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88169232-T-A

233804971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88169233-G-A

233804971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88169233-G-T

233804985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88169247-A-G

233804987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88169249-G-A

233804987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88169249-G-T

233805018-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: synonymous variant
orthologous variants: 88169279-C-G

233805018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: synonymous variant
orthologous variants: 88169279-C-T

233805031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense variant
orthologous variants: 88169292-C-T

233805045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: stop gained
orthologous variants: 88169306-G-A

233805081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: synonymous variant
orthologous variants: 88169342-T-C

233805081-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense variant
orthologous variants: 88169342-T-G

http://identifiers.org/hco/2/GRCh38#233805087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88169348-C-A

233805087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: synonymous variant
orthologous variants: 88169348-C-T

233805116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88169377-G-A

233805116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88169377-G-T

http://identifiers.org/hco/2/GRCh38#233805129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88169390-C-A

233805129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88169390-C-T

233805133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88169394-A-G

233805138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88169399-T-C

233805146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88169416-G-A

233805146-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88169416-G-C

233805146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88169416-G-T

http://identifiers.org/hco/2/GRCh38#233805157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88169427-C-A

233805157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88169427-C-T

233805173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88169454-G-A

233805173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88169454-G-T

233805238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88169519-G-T

http://identifiers.org/hco/2/GRCh38#233805417-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88169683-A-C

233806599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88169812-A-G

233806617-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88169830-C-G

233806617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88169830-C-T

233806690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88169905-C-T

233807342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88170047-G-A

233807342-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88170047-G-C

233807342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88170047-G-T

http://identifiers.org/hco/2/GRCh38#233807352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88170057-C-A

233807352-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88170057-C-G

233807374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88170078-G-A

233807374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88170078-G-T

233807436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense variant
orthologous variants: 88170139-G-A

233807436-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense variant
orthologous variants: 88170139-G-C

233807436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense variant
orthologous variants: 88170139-G-T

http://identifiers.org/hco/2/GRCh38#233807439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88170142-C-A

233807439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense variant
orthologous variants: 88170142-C-T

http://identifiers.org/hco/2/GRCh38#233807440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88170143-C-A

233807440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: synonymous variant
orthologous variants: 88170143-C-T

233807519-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense variant
orthologous variants: 88170222-T-G

http://identifiers.org/hco/2/GRCh38#233807530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88170233-C-A

233807530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: synonymous variant
orthologous variants: 88170233-C-T

http://identifiers.org/hco/2/GRCh38#233807537-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88170240-A-C

233807538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense variant
orthologous variants: 88170241-G-A

233807549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 88170252-G-T

233807552-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88170255-C-G

233807552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88170255-C-T

233807556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88170259-C-T

http://identifiers.org/hco/2/GRCh38#233807557-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88170260-A-C

233807557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88170260-A-G

http://identifiers.org/hco/2/GRCh38#233807562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88170264-C-A

233807562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88170264-C-T

http://identifiers.org/hco/2/GRCh38#233807592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88170298-C-A

233807592-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88170298-C-G

233807592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88170298-C-T

233807593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88170299-G-A

233807593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88170299-G-T

233807623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88170315-G-A

233807636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88170328-G-A

233807715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88170377-G-A

233807756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 88170414-G-A

http://identifiers.org/hco/2/GRCh38#233807763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88170421-C-A

233807763-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant
orthologous variants: 88170421-C-G

233807763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant
orthologous variants: 88170421-C-T

233807764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 88170422-G-A

233807764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 88170422-G-T

233807822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: synonymous variant
orthologous variants: 88170480-G-A

233807824-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: stop gained
orthologous variants: 88170482-C-G

233807827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense variant
orthologous variants: 88170485-A-G

233807828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: synonymous variant
orthologous variants: 88170486-G-A

233807871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88170529-T-C

233809134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 88171661-T-C

233809144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant
orthologous variants: 88171671-C-T

233809145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant
orthologous variants: 88171672-G-A

233809145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant
orthologous variants: 88171672-G-T

233809164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 88171691-C-T

233809185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 88171712-C-T

233809197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 88171724-C-T

http://identifiers.org/hco/2/GRCh38#233809206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88171733-C-A

233809206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 88171733-C-T

233809209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant
orthologous variants: 88171736-G-T

233809239-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant
orthologous variants: 88171766-C-G

233809266-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 88171793-C-G

233809306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant
orthologous variants: 88171824-G-A

233809325-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, splice_donor_variant
orthologous variants: 88171840-T-G

233809342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88171850-G-A

233809382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88171868-A-G

233809410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88171879-G-A

233809410-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88171879-G-C

233809410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88171879-G-T

http://identifiers.org/hco/2/GRCh38#233809417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88171886-C-A

233809421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88171890-G-A

233809421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88171890-G-T

233809437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88171896-C-T

233809650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88172066-A-G

233810642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88172509-G-A

233810660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88172530-G-A

233810660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88172530-G-T

http://identifiers.org/hco/2/GRCh38#233810675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88172545-C-A

233810696-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88172566-T-A

http://identifiers.org/hco/2/GRCh38#233810743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88172615-C-A

http://identifiers.org/hco/2/GRCh38#233810759-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88172631-A-C

http://identifiers.org/hco/2/GRCh38#233810789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88172661-C-A

233810789-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 88172661-C-G

233810945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88172814-C-T

233810976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88172848-G-A

233810976-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88172848-G-C

233810983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88172855-G-T

233811230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88173096-G-A

233811354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88173210-C-T

http://identifiers.org/hco/2/GRCh38#233811393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88173239-C-A

233811412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88173249-G-A

233811524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88173367-G-A

233811662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88173483-T-C

233811751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88173553-A-G

233811790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88173589-G-A

233811790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88173589-G-T

http://identifiers.org/hco/2/GRCh38#233811831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88173641-C-A

233811831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88173641-C-T

http://identifiers.org/hco/2/GRCh38#233811832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88173642-C-A

233811832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88173642-C-T

233811868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88173698-T-C

233811874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 88173704-G-T

233811881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 88173711-C-T

233811900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: synonymous variant
orthologous variants: 88173730-G-A

233811900-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: synonymous variant
orthologous variants: 88173730-G-C

233811900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: synonymous variant
orthologous variants: 88173730-G-T

233811909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: synonymous variant
orthologous variants: 88173739-C-T

233811922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense variant
orthologous variants: 88173752-G-A

http://identifiers.org/hco/2/GRCh38#233811929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88173759-C-A

233811929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense variant
orthologous variants: 88173759-C-T

233811943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense variant
orthologous variants: 88173773-G-A

233811943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense variant
orthologous variants: 88173773-G-T

233811944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense variant
orthologous variants: 88173774-C-T

233811957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 88173787-G-T

233811960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: splice donor variant
orthologous variants: 88173790-G-A

http://identifiers.org/hco/2/GRCh38#233812015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88173854-C-A

233812015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88173854-C-T

233812016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88173855-A-G

233812016-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88173855-A-T

http://identifiers.org/hco/2/GRCh38#233812027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88173878-C-A

233812027-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88173878-C-G

233812027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88173878-C-T

233812075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88173913-G-A

233812075-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88173913-G-C

233812075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88173913-G-T

233812076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88173914-G-A

233812076-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88173914-G-C

233812076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88173914-G-T

http://identifiers.org/hco/2/GRCh38#233812091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88173929-C-A

233812091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88173929-C-T

http://identifiers.org/hco/2/GRCh38#233812095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88173933-C-A

233812095-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88173933-C-G

233812095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88173933-C-T

233812798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88174239-G-A

233812919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88174366-G-A

233812919-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88174366-G-C

233812919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88174366-G-T

233812925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88174372-G-A

233812959-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88174420-C-G

233813063-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88174540-T-A

233813431-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88174627-G-C

233813495-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88174690-C-G

233813509-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88174700-G-C

233813516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88174707-G-A

233813531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88174722-A-G

233813553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88174744-G-A

233813559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88174750-G-T

233813577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88174769-T-C

233813593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88174785-G-A

http://identifiers.org/hco/2/GRCh38#233813594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88174787-C-A

http://identifiers.org/hco/2/GRCh38#233813595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88174788-C-A

233813595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88174788-C-T

233813612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88174804-G-A

233813612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88174804-G-T

233813673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: synonymous variant
orthologous variants: 88174861-G-A

http://identifiers.org/hco/2/GRCh38#233813674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88174862-C-A

http://identifiers.org/hco/2/GRCh38#233813746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88174934-C-A

http://identifiers.org/hco/2/GRCh38#233813752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88174940-C-A

233813766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: synonymous variant
orthologous variants: 88174954-T-C

233813767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: stop gained
orthologous variants: 88174955-G-T

http://identifiers.org/hco/2/GRCh38#233813771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88174959-C-A

233813783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88174976-G-A

233813791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88174984-G-A

233813796-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88174989-G-C

233813800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88174996-C-T

233814009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88175154-C-T

233814083-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88175226-T-G

233814097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88175240-G-A

233814124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88175261-G-A

233814597-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense variant
orthologous variants: 88175485-G-C

233814597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense variant
orthologous variants: 88175485-G-T

http://identifiers.org/hco/2/GRCh38#233814731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88175622-C-A

233814748-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88175639-C-G

233814748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88175639-C-T

http://identifiers.org/hco/2/GRCh38#233814750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88175641-C-A

233814751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88175642-T-C

233814752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88175643-G-A

233814752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88175643-G-T

233816577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88176056-C-T

233816592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88176071-G-A

233816631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88176107-C-T

233816632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88176108-A-G

233816632-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88176108-A-T

http://identifiers.org/hco/2/GRCh38#233816652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88176139-C-A

http://identifiers.org/hco/2/GRCh38#233816662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88176149-C-A

233816662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88176149-C-T

http://identifiers.org/hco/2/GRCh38#233816674-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88176162-A-C

233816674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88176162-A-G

233816678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88176166-A-G

233816678-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88176166-A-T

233816700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88176194-T-C

233816701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88176195-G-A

233816701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88176195-G-T

233816702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88176196-A-G

233816702-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88176196-A-T

233816726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88176216-A-G

233816754-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88176247-C-G

233816754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88176247-C-T

233816759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88176252-G-A

233816759-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88176252-G-C

233816759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88176252-G-T

233816784-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant
orthologous variants: 88176277-C-G

233816794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant
orthologous variants: 88176287-G-T

233816813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 88176306-A-G

233816815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, stop_gained
orthologous variants: 88176308-G-A

http://identifiers.org/hco/2/GRCh38#233816831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88176324-C-A

233816831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 88176324-C-T

233816850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant
orthologous variants: 88176343-C-T

233816864-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, stop_gained
orthologous variants: 88176357-T-A

233816884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 88176377-G-A

233816884-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 88176377-G-C

233816884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 88176377-G-T

233816984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88176484-G-A

http://identifiers.org/hco/2/GRCh38#233816993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88176492-C-A

233816993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88176492-C-T

233817007-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88176506-G-T

233817021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88176520-T-C

233817021-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88176520-T-G

http://identifiers.org/hco/2/GRCh38#233817032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88176538-C-A

233817032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88176538-C-T

233817037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88176543-G-T

233817056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88176561-G-A

233817060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88176565-G-A

233817061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88176566-G-T

233817114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88176620-G-A

http://identifiers.org/hco/2/GRCh38#233817244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88176718-C-A

233817244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88176718-C-T

233817378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88176849-G-A

233817548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88177002-T-C

233817587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88177054-G-T

233817685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88177142-A-G

233817691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88177148-G-T

http://identifiers.org/hco/2/GRCh38#233817858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88177320-C-A

233817858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88177320-C-T

233817909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88177339-G-A

233817909-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88177339-G-C

233817909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88177339-G-T

233817945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88177368-G-A

233817985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88177408-G-A

233817993-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88177416-G-C

http://identifiers.org/hco/2/GRCh38#233817999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88177422-C-A

233818039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant
orthologous variants: 88177462-G-A

233818043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 88177466-C-T

233818064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 88177487-T-C

233818071-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant
orthologous variants: 88177494-C-G

233818097-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant
orthologous variants: 88177520-T-A

233818097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 88177520-T-C

233818097-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant
orthologous variants: 88177520-T-G

233818139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88177563-G-A

233818139-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88177563-G-T

233818151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88177575-C-T

233818172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88177591-A-G

233818189-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88177603-T-A

233818189-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88177603-T-G

233818194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88177604-G-A

233818194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88177604-G-T

233818256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88177663-G-A

233818287-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88177692-T-G

233818454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88177841-C-T

233818517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88177902-G-T

http://identifiers.org/hco/2/GRCh38#233818541-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88177926-A-C

233818541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88177926-A-G

233818639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88177974-G-A

233818639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88177974-G-T

233818653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, splice_region_variant, synonymous_variant
orthologous variants: 88177988-A-G

233818655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant
orthologous variants: 88177990-G-A

http://identifiers.org/hco/2/GRCh38#233818661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88177996-C-A

233818729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant
orthologous variants: 88178064-G-A

233818729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant
orthologous variants: 88178064-G-T

233818732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant
orthologous variants: 88178067-G-A

233818757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant
orthologous variants: 88178092-C-T

233818765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant
orthologous variants: 88178100-G-A

233818771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, splice_donor_variant
orthologous variants: 88178106-G-T

233818780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88178115-G-A

233818780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88178115-G-T

233818781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88178126-G-A

http://identifiers.org/hco/2/GRCh38#233818796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88178138-C-A

233818796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88178138-C-T

233818805-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88178147-T-A

233818806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88178148-G-A

233818806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88178148-G-T

233818815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88178157-G-A

http://identifiers.org/hco/2/GRCh38#233818816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88178158-C-A

233819064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88178699-C-T

233819083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88178717-C-T

http://identifiers.org/hco/2/GRCh38#233819169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88178808-C-A

233819197-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88178827-C-G

233819209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88178839-G-A

233819209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88178839-G-T

233819235-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88178875-T-A

233819235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88178875-T-C

233819235-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88178875-T-G

233819238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88178895-G-A

233819238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88178895-G-T

233819301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88178951-C-T

233819318-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 88178968-T-A

233819318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 88178968-T-C

233819343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 88178993-T-C

233819361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 88179011-C-T

233819410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant
orthologous variants: 88179060-G-T

http://identifiers.org/hco/2/GRCh38#233819437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88179087-C-A

233819437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant
orthologous variants: 88179087-C-T

http://identifiers.org/hco/2/GRCh38#233819446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88179096-C-A

233819446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant
orthologous variants: 88179096-C-T

233819448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 88179098-G-T

233819457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant
orthologous variants: 88179107-G-T

233819517-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88179161-T-A

233819517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88179161-T-C

233819564-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88179175-C-G

http://identifiers.org/hco/2/GRCh38#233819578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88179194-C-A

233819578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88179194-C-T

http://identifiers.org/hco/2/GRCh38#233819585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88179201-C-A

233819585-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88179201-C-G

http://identifiers.org/hco/2/GRCh38#233819593-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88179209-C-A

233819601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88179214-G-A

233819601-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88179214-G-C

233819601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88179214-G-T

233819668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88179276-G-A

http://identifiers.org/hco/2/GRCh38#233819725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88179325-C-A

233819757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88179353-G-A

233819757-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88179353-G-C

233819757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88179353-G-T

http://identifiers.org/hco/2/GRCh38#233819764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88179360-C-A

233819771-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88179367-G-C

233819771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88179367-G-T

233819777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88179381-T-C

233819790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88179394-T-C

233819790-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88179394-T-G

http://identifiers.org/hco/2/GRCh38#233819873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88180025-C-A

233819873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88180025-C-T

233819880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88180035-G-A

233819880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88180035-G-T

http://identifiers.org/hco/2/GRCh38#233819914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88180070-C-A

233819914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 88180070-C-T

http://identifiers.org/hco/2/GRCh38#233819949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88180105-C-A

233819949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 88180105-C-T

233819982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 88180138-C-T

233820000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 88180156-C-T

http://identifiers.org/hco/2/GRCh38#233820023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88180179-C-A

233820023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant
orthologous variants: 88180179-C-T

http://identifiers.org/hco/2/GRCh38#233820024-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88180180-A-C

233820024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 88180180-A-G

233820301-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88180391-C-G

233820319-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88180422-G-C

233820558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88180726-G-A

233820621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88180845-G-A

http://identifiers.org/hco/2/GRCh38#233820707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88180911-C-A

233820710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88180914-A-G

233820735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88180963-A-G

233820783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88181017-A-G

233821061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88181304-G-A

233821157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88181388-A-G

233821210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88181441-C-T

233821353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88181550-C-T

233821395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88181595-G-T

233821569-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88181745-C-G

http://identifiers.org/hco/2/GRCh38#233821720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88182117-C-A

233821798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88182298-G-A

233821829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88182326-C-T

http://identifiers.org/hco/2/GRCh38#233821899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88182398-C-A

233822048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88182505-A-G

233822051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88182508-G-T

233822057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88182515-A-G

233822076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88182534-G-T

233822097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88182556-C-T

233822111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88182567-T-C

233822152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant
orthologous variants: 88182608-T-C

http://identifiers.org/hco/2/GRCh38#233822169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88182625-C-A

233822169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 88182625-C-T

233822170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant
orthologous variants: 88182626-G-A

233822170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant
orthologous variants: 88182626-G-T

233822172-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 88182628-C-G

233822172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 88182628-C-T

233822201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant
orthologous variants: 88182657-G-A

233822214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 88182670-G-T

233822231-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant
orthologous variants: 88182687-G-C

233822231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant
orthologous variants: 88182687-G-T

233822266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant
orthologous variants: 88182722-G-A

233822266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant
orthologous variants: 88182722-G-T

233822304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88182760-C-T

233822306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88182762-A-G

233822322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88182777-C-T

233822364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 88182813-C-T

233822402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant
orthologous variants: 88182851-G-A

233822402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, stop_gained
orthologous variants: 88182851-G-T

http://identifiers.org/hco/2/GRCh38#233822446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88182895-C-A

233822446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 88182895-C-T

233822477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant
orthologous variants: 88182926-C-T

http://identifiers.org/hco/2/GRCh38#233822548-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88182997-C-A

233822586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88183052-G-T

233822619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88183085-C-T

233822631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88183097-G-A

233822631-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88183097-G-C

233822631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88183097-G-T

http://identifiers.org/hco/2/GRCh38#233822692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88183149-C-A

233822692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88183149-C-T

233822695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88183152-T-C

233822702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88183160-T-C

233822702-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88183160-T-G

233822741-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88183198-A-T

http://identifiers.org/hco/2/GRCh38#233822742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88183199-C-A

233822904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant
orthologous variants: 88183288-T-C

233822945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 88183329-C-T

233822971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 88183355-C-T

233822980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 88183364-C-T

233823020-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, splice_donor_variant
orthologous variants: 88183404-T-A

233823160-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88183518-T-A

233823160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88183518-T-C

233823319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88183584-C-T

233823463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88183686-G-A

233823463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88183686-G-T

233823467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88183690-A-G

233823467-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88183690-A-T

http://identifiers.org/hco/2/GRCh38#233823472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88183699-C-A

233823472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88183699-C-T

233823518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88183743-G-A

233823521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88183746-C-T

233823522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88183747-G-A

233823522-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88183747-G-C

233823526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88183751-C-T

233823550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 88183773-C-T

233823654-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant
orthologous variants: 88183877-C-G

233823654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant
orthologous variants: 88183877-C-T

233823702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88183935-G-A

233823702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88183935-G-T

233823703-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88183939-G-C

233823749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88183983-G-A

233823749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88183983-G-T

http://identifiers.org/hco/2/GRCh38#233823786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88184032-C-A

233823786-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88184032-C-G

http://identifiers.org/hco/2/GRCh38#233823799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88184045-C-A

233823800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88184046-T-C

233823802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron variant
orthologous variants: 88184048-T-C

http://identifiers.org/hco/2/GRCh38#233828622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88184114-C-A

233828622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 88184114-C-T

http://identifiers.org/hco/2/GRCh38#233828638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88184130-C-A

233828638-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88184130-C-G

233828638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88184130-C-T

233828652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88184144-A-G

233828674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88184166-G-A

233828698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88184190-T-C

233828734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88184226-G-A

233828734-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88184226-G-C

233828734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88184226-G-T

233828742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88184234-G-A

233828752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88184244-C-T

233828775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88184267-A-G

233828795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88184286-C-T

233828830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88184314-G-A

233828830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88184314-G-T

http://identifiers.org/hco/2/GRCh38#233828835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88184319-C-A

233828835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88184319-C-T

http://identifiers.org/hco/2/GRCh38#233828845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88184329-C-A

233828845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88184329-C-T

http://identifiers.org/hco/2/GRCh38#233828944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88184427-C-A

233828944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88184427-C-T

233828960-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88184443-T-G

233828961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88184444-G-A

http://identifiers.org/hco/2/GRCh38#233828967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88184450-C-A

233828967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88184450-C-T

http://identifiers.org/hco/2/GRCh38#233828988-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88184471-C-A

http://identifiers.org/hco/2/GRCh38#233829007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88184490-C-A

233829007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88184490-C-T

233829008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88184491-G-A

233829008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88184491-G-T

233829016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88184499-G-A

233829016-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88184499-G-C

233829016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88184499-G-T

http://identifiers.org/hco/2/GRCh38#233829027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88184510-C-A

233829027-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88184510-C-G

233829037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88184520-G-A

233829149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88184966-T-C

233829163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88184979-G-A

233829163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88184979-G-T

233829306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88185117-G-A

233829307-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88185118-G-C

233829468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88185289-C-T

233829469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88185290-G-A

233829469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88185290-G-T

233829477-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88185296-T-G

http://identifiers.org/hco/2/GRCh38#233829480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88185299-C-A

233829480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88185299-C-T

http://identifiers.org/hco/2/GRCh38#233829521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88185338-C-A

233829526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88185343-G-A

233829526-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88185343-G-C

233829526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88185343-G-T

233829551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88185369-G-T

233829565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88185383-G-A

233829565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88185383-G-T

http://identifiers.org/hco/2/GRCh38#233829595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88185405-C-A

233829595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88185405-C-T

233829626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88185438-G-A

233829636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88185448-G-A

233829636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88185448-G-T

http://identifiers.org/hco/2/GRCh38#233829649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88185461-C-A

233829649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88185461-C-T

233829668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88185480-G-A

233829668-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88185480-G-C

233829668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88185480-G-T

233829694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88185506-G-T

233829712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88185524-G-A

233829712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88185524-G-T

233829715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88185527-G-A

233829717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88185529-A-G

233829782-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 88185594-T-A

233829782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 88185594-T-C

233829799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88185611-G-A

233829799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88185611-G-T

http://identifiers.org/hco/2/GRCh38#233829801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88185613-C-A

233829801-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88185613-C-G

233829801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88185613-C-T

233829818-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88185631-T-A

233829818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88185631-T-C

233829818-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88185631-T-G

http://identifiers.org/hco/2/GRCh38#233829865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88185680-C-A

http://identifiers.org/hco/2/GRCh38#233829874-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88185689-C-A

233829874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88185689-C-T

233829886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88185701-T-C

233829886-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88185701-T-G

233830020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88185783-G-A

233830020-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88185783-G-C

233830020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88185783-G-T

http://identifiers.org/hco/2/GRCh38#233831279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88186182-C-A

233831319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88186220-G-A

233831321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88186222-G-T

233831329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88186230-C-T

233831369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88186260-G-A

233831369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88186260-G-T

233831379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88186273-T-C

233831380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88186274-G-A

233831384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88186278-C-T

233831398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88186294-T-C

233831398-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88186294-T-G

233831448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88186344-G-A

233831448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88186344-G-T

http://identifiers.org/hco/2/GRCh38#233831459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88186355-C-A

233831459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88186355-C-T

233831486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88186382-T-C

233831490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88186386-G-A

233831490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88186386-G-T

233831534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88186430-C-T

http://identifiers.org/hco/2/GRCh38#233831538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88186434-C-A

233831549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88186445-G-A

233831549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88186445-G-T

233831600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88186452-G-T

233831601-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88186453-G-C

233831601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88186453-G-T

233831613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88186465-T-C

http://identifiers.org/hco/2/GRCh38#233831634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88186476-C-A

233831634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88186476-C-T

233831639-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88186481-T-A

233831639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88186481-T-C

233831848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88186662-G-A

233831869-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88186694-G-C

http://identifiers.org/hco/2/GRCh38#233832293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88186952-C-A

233832293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88186952-C-T

233832294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88186953-G-A

233832313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88186972-A-G

http://identifiers.org/hco/2/GRCh38#233832341-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88186999-C-A

233832341-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88186999-C-G

233832341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88186999-C-T

233832378-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88187040-T-A

233832378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88187040-T-C

233832379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88187041-G-A

233832383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88187048-A-G

http://identifiers.org/hco/2/GRCh38#233832390-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#88187055-A-C

233832390-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88187055-A-T

233832394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88187059-G-T

233832412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88187080-T-C

233832419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88187087-T-C

233832419-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88187087-T-G

233832423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88187091-T-C

http://identifiers.org/hco/2/GRCh38#233832493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88187147-C-A

233832493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88187147-C-T

233832495-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88187149-T-A

233832495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88187149-T-C

233832504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 88187158-G-A

233832504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 88187158-G-T

http://identifiers.org/hco/2/GRCh38#233832524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88187192-C-A

233832551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88187223-A-G

233832586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88187259-T-C

233832586-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88187259-T-G

233832616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88187289-A-G

233832638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 88187311-C-T

233832639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 88187312-G-A

233832640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 88187313-G-T

233832655-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88187329-G-C

233832758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88187394-G-A

233832758-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88187394-G-C

233832758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88187394-G-T

233832765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88187400-G-A

233832765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88187400-G-T

233832778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88187413-G-A

233832778-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88187413-G-C

233832778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88187413-G-T

233832782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88187418-G-T

http://identifiers.org/hco/2/GRCh38#233832864-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88187473-A-C

233832929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88187493-T-C

http://identifiers.org/hco/2/GRCh38#233833027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#88187555-C-A

233833027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88187555-C-T

233833028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88187556-T-C

233833029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88187557-G-A

233833029-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88187557-G-C

233833029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88187557-G-T

http://identifiers.org/hco/2/GRCh38#233833030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#88187558-C-A

233833030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88187558-C-T

http://identifiers.org/hco/2/GRCh38#233833044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#88187565-C-A

233833084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88187583-A-G

233833146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 88187635-G-A

233833146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: non_coding_transcript_exon_variant, stop_gained, undefined
orthologous variants: 88187635-G-T

http://identifiers.org/hco/2/GRCh38#233833155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#88187644-C-A

233833155-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 88187644-C-G

233833196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88187685-G-A

233833196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88187685-G-T

233833203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88187692-G-A

233833235-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 88187724-G-C

http://identifiers.org/hco/2/GRCh38#233833273-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88187762-A-C

233833273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88187762-A-G

233833280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88187766-A-G

233833284-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88187770-T-G

http://identifiers.org/hco/2/GRCh38#233833287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88187773-C-A

233833287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88187773-C-T

233833359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88187834-G-A

233833398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27936
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88187873-T-C