27491055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, undefined
orthologous variants: 66362050-A-G

27491055-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, undefined
orthologous variants: 66362050-A-T

27491143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 66361958-G-A

27491143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 66361958-G-T

27491179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 66361917-G-A

27491179-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 66361917-G-T

27491196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 66361896-C-T

27491221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 66361870-G-T

27491227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 66361864-G-A

27491227-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 66361864-G-C

27491227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 66361864-G-T

27491338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66361765-T-C

27491366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 66361738-G-A

27491366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 66361738-G-T

http://identifiers.org/hco/8/GRCh38#27491367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#66361737-C-A

27491367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 66361737-C-T

27491370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 66361734-G-T

27491371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 66361733-G-A

27491609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 66361531-C-T

27499425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66356282-G-A

27500942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 66354226-G-A

27501054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66354120-C-T

27503535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66347801-G-A

http://identifiers.org/hco/8/GRCh38#27503546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#66347791-C-A

27503781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66347545-G-A

27503781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66347545-G-T

27503789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66347537-C-T

27503819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66347506-A-G

http://identifiers.org/hco/8/GRCh38#27503898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#66347446-C-A

27503948-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66347396-G-C

27504148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66347198-A-G

27504158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66347188-A-G

27504223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66347123-A-G

27504280-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66347077-C-G

27504447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66346562-C-T

27504616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66345958-G-A

27504689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66345877-C-T

27504720-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66345851-C-G

27504819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66345765-G-T

27504824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66345760-A-G

http://identifiers.org/hco/8/GRCh38#27504883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#66345691-C-A

27504883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66345691-C-T

27504886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66345688-T-C

27504886-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66345688-T-G

27504999-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 66345571-T-G

27505007-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 66345563-G-C

27505057-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 66345513-C-G

27505057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 66345513-C-T

27505166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66345404-T-C

http://identifiers.org/hco/8/GRCh38#27505240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#66345328-C-A

27505477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66345155-C-T

27505506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66345127-G-A

27505580-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66345038-C-G

27507002-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, stop_lost
orthologous variants: 66344653-G-C

27511419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66341595-C-T

http://identifiers.org/hco/8/GRCh38#27511529-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#66341482-A-C

27511626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66341398-C-T

27511857-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 66341226-C-G

27511857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 66341226-C-T

27515408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66339979-A-G

27515442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66339945-G-A

27515442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66339945-G-T

http://identifiers.org/hco/8/GRCh38#27515661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#66339744-C-A

27515661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66339744-C-T

27515663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66339736-T-C

27515886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 66339544-A-G

27515964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 66339489-C-T

27516072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66339384-A-G

http://identifiers.org/hco/8/GRCh38#27516271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#66339173-C-A

27516271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66339173-C-T

27516424-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66339007-T-A

27516469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66338958-G-A

27516469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66338958-G-T

27516502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66338925-C-T

http://identifiers.org/hco/8/GRCh38#27516540-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#66338880-A-C

27516540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66338880-A-G

27516540-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66338880-A-T

27516642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66338786-A-G

27518090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 66336233-T-C

27518154-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66336160-T-G

27518247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66336069-G-A

27520947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66333095-C-T

27521389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66332780-G-A

27522307-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66332377-T-G

27522457-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 66332236-G-C

27523235-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66331693-A-T

http://identifiers.org/hco/8/GRCh38#27523294-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#66331636-A-C

27523314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66331616-G-T

27523358-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66331584-T-G

27523414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66331531-C-T

27523514-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66331444-T-A

27523835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66330898-G-A

27525110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66330587-G-A

27525114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66330583-G-A

27525114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66330583-G-T

27525218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66330494-A-G

27525286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66330425-A-G

http://identifiers.org/hco/8/GRCh38#27525290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#66330421-C-A

27525342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66330377-G-A

27525363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 66330356-G-A

27525524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66330201-C-T

http://identifiers.org/hco/8/GRCh38#27525578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#66330117-C-A

http://identifiers.org/hco/8/GRCh38#27525622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#66330074-C-A

27525622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66330074-C-T

27525808-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66329860-T-G

http://identifiers.org/hco/8/GRCh38#27525863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#66329815-C-A

27536187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66327455-A-G

http://identifiers.org/hco/8/GRCh38#27536653-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#66327167-A-C

27536653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66327167-A-G

27536709-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66327106-T-G

27536853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 66326958-G-A

27538057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66326750-C-T

27538181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66326627-A-G

27538210-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66326594-T-A

27538210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66326594-T-C

27538262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66326540-C-T

27538426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66326154-G-A

27538432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66326148-G-A

27538432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66326148-G-T

27538512-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66325980-C-G

27538512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66325980-C-T

http://identifiers.org/hco/8/GRCh38#27538518-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#66325974-A-C

27538518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66325974-A-G

27538518-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66325974-A-T

27538520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66325972-T-C

27538526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66325966-G-A

27538546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66325929-T-C

27538579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66325887-G-A

27538611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66325819-T-C

27538611-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66325819-T-G

27538621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66325809-A-G

http://identifiers.org/hco/8/GRCh38#27538625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#66325805-C-A

27538625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66325805-C-T

27538808-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66325619-T-G

http://identifiers.org/hco/8/GRCh38#27538811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#66325616-C-A

27538844-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66325583-A-T

27538846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66325581-T-C

http://identifiers.org/hco/8/GRCh38#27538884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#66325571-C-A

27538909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66325555-A-G

27538909-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66325555-A-T

27538930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66325533-G-A

27538930-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66325533-G-C

27538931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66325532-A-G

http://identifiers.org/hco/8/GRCh38#27538950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#66325522-C-A

27538950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66325522-C-T

27538972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66325497-T-C

27538972-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66325497-T-G

27538986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66325483-G-A

27538986-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66325483-G-C

27538986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66325483-G-T

27538989-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66325480-T-A

27539006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66325447-T-C

27539025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66325428-G-A

27539025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66325428-G-T

http://identifiers.org/hco/8/GRCh38#27539058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#66325396-C-A

27539058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66325396-C-T

27539059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66325395-T-C

27539124-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66325307-G-T

http://identifiers.org/hco/8/GRCh38#27539195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#66325273-C-A

27539195-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66325273-C-G

http://identifiers.org/hco/8/GRCh38#27539212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#66325256-C-A

27539212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66325256-C-T

http://identifiers.org/hco/8/GRCh38#27539398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#66325155-C-A

27539398-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66325155-C-G

27539416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66325133-A-G

27539581-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66325008-C-G

http://identifiers.org/hco/8/GRCh38#27539863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#66324786-C-A

27540585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 66324483-C-T

27540722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66324362-A-G

27540767-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66324328-A-T

27540801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66324290-T-C

27540801-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66324290-T-G

27540924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66324176-C-T

27541081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66324070-C-T

27541130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66324019-T-C

27543622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66322986-G-A

27543622-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66322986-G-T

27543688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66322909-G-A

27543794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 66322778-C-T

27543857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 66322715-A-G

27543882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 66322702-G-A

27543882-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 66322702-G-C

27543882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 66322702-G-T

27543884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 66322700-G-T

27544039-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66322595-T-G

27544062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66322572-T-C

http://identifiers.org/hco/8/GRCh38#27544114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#66322509-C-A

27544114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66322509-C-T

27544329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66322297-T-C

27544329-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66322297-T-G

27544407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66322229-T-C

27544620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66322084-G-A

27544620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66322084-G-T

http://identifiers.org/hco/8/GRCh38#27544693-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#66322019-A-C

27544693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66322019-A-G

27544722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66321992-T-C

http://identifiers.org/hco/8/GRCh38#27544832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#66321914-C-A

27544832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66321914-C-T

27544888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66321855-A-G

27544888-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66321855-A-T

27544910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66321833-G-A

http://identifiers.org/hco/8/GRCh38#27544927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#66321818-C-A

27544945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 66321801-A-G

27544945-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 66321801-A-T

27544953-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 66321793-T-G

27545374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 66321505-G-A

27545374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 66321505-G-T

http://identifiers.org/hco/8/GRCh38#27545384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#66321495-C-A

27545384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 66321495-C-T

http://identifiers.org/hco/8/GRCh38#27545465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#66321413-C-A

27545465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 66321413-C-T

http://identifiers.org/hco/8/GRCh38#27545547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#66321336-C-A

27545588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron variant
orthologous variants: 66321273-G-A

27545588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron variant
orthologous variants: 66321273-G-T

http://identifiers.org/hco/8/GRCh38#27545594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#66321267-C-A

http://identifiers.org/hco/8/GRCh38#27545605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#66321256-C-A

27545648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3402
most severe consequence: intron variant
orthologous variants: 66321212-C-T