27878492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 78730879-G-A

http://identifiers.org/hco/17/GRCh38#27878575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#78730812-C-A

27878575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 78730812-C-T

http://identifiers.org/hco/17/GRCh38#27878577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#78730810-C-A

http://identifiers.org/hco/17/GRCh38#27878585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#78730802-C-A

27878622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 78730788-A-G

27878676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 78730735-G-T

27878704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 78730707-G-T

27878705-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 78730706-T-A

27878705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 78730706-T-C

27878822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 78730629-G-A

27878822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 78730629-G-T

http://identifiers.org/hco/17/GRCh38#27878823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#78730628-C-A

27878823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 78730628-C-T

27878842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 78730604-G-A

27878842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 78730604-G-T

27878845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 78730601-G-T

27878854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 78730592-G-A

27878854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 78730592-G-T

http://identifiers.org/hco/17/GRCh38#27878855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#78730591-C-A

27878863-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 78730583-A-T

27878872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 78730574-G-A

27878872-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 78730574-G-C

27878872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 78730574-G-T

27878882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 78730564-A-G

27878901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 78730546-G-A

27878901-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 78730546-G-C

27878901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 78730546-G-T

27878929-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 78730523-T-A

27878929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 78730523-T-C

27878955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 78730501-G-T

27878971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 78730485-G-A

27878971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 78730485-G-T

http://identifiers.org/hco/17/GRCh38#27878993-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#78730464-A-C

27878993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 78730464-A-G

http://identifiers.org/hco/17/GRCh38#27879084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#78730356-C-A

http://identifiers.org/hco/17/GRCh38#27879086-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#78730354-C-A

27879132-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78730308-C-G

http://identifiers.org/hco/17/GRCh38#27879146-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#78730294-A-C

27879261-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78730179-T-A

27879261-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78730179-T-G

http://identifiers.org/hco/17/GRCh38#27879265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#78730175-C-A

27879266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78730174-A-G

http://identifiers.org/hco/17/GRCh38#27879343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#78730096-C-A

27879343-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78730096-C-G

27879378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78730067-A-G

27879378-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78730067-A-T

27879392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78730053-T-C

27879427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78730024-G-A

27879427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78730024-G-T

27879452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78729990-G-A

27879452-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78729990-G-C

27879452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78729990-G-T

27879454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78729988-A-G

27879454-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78729988-A-T

27879458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78729984-T-C

27879460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78729982-A-G

27879460-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78729982-A-T

http://identifiers.org/hco/17/GRCh38#27879461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#78729981-C-A

27879461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78729981-C-T

27879483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 78729954-T-C

27879540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78729902-G-A

27879572-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78729884-T-A

27879593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78729865-G-A

27879593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78729865-G-T

27879624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78729834-G-T

27879655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78729805-T-C

27879655-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78729805-T-G

http://identifiers.org/hco/17/GRCh38#27879660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#78729800-C-A

27879684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78729779-G-A

27879684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78729779-G-T

http://identifiers.org/hco/17/GRCh38#27879695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#78729764-C-A

27879695-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78729764-C-G

27879695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78729764-C-T

27879698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78729761-A-G

27880150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 78729154-G-A

27880150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 78729154-G-T

http://identifiers.org/hco/17/GRCh38#27880174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#78729096-C-A

27880174-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 78729096-C-G

27880174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 78729096-C-T

27880210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 78729060-G-T

27880215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 78729055-G-A

27880215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 78729055-G-T

http://identifiers.org/hco/17/GRCh38#27880234-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#78729037-A-C

27880276-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: 78729004-T-A

27880276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 78729004-T-C

27880276-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 78729004-T-G

27880350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 78728930-G-A

27880350-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 78728930-G-C

27880350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 78728930-G-T

http://identifiers.org/hco/17/GRCh38#27880380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#78728900-C-A

27880380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78728900-C-T

27880387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78728893-A-G

http://identifiers.org/hco/17/GRCh38#27880451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#78728843-C-A

http://identifiers.org/hco/17/GRCh38#27880509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#78728801-C-A

27880559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78728772-T-C

27880578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78728753-G-A

27880582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78728749-G-A

27880582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78728749-G-T

27880611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78728721-G-A

27880611-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78728721-G-C

27880611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78728721-G-T

27880749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78728619-G-A

27880749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78728619-G-T

27880781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78728583-T-C

http://identifiers.org/hco/17/GRCh38#27880806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#78728559-C-A

27880806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78728559-C-T

27880838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78728527-T-C

27881768-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron variant
orthologous variants: 78727548-T-A

27881774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron variant
orthologous variants: 78727542-G-T

27881961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron variant
orthologous variants: 78727349-G-A

27881965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron variant
orthologous variants: 78727345-C-T

27882383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron variant
orthologous variants: 78727136-G-A

http://identifiers.org/hco/17/GRCh38#27882460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#78727066-C-A

27882460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron variant
orthologous variants: 78727066-C-T

27882465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron variant
orthologous variants: 78727061-C-T

http://identifiers.org/hco/17/GRCh38#27882492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#78727044-C-A

http://identifiers.org/hco/17/GRCh38#27882505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#78727031-C-A

27882505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron variant
orthologous variants: 78727031-C-T

27882506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron variant
orthologous variants: 78727030-T-C

27882506-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron variant
orthologous variants: 78727030-T-G

27882507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron variant
orthologous variants: 78727029-G-A

27882507-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron variant
orthologous variants: 78727029-G-C

27882507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron variant
orthologous variants: 78727029-G-T

http://identifiers.org/hco/17/GRCh38#27882510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#78727026-C-A

27882510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron variant
orthologous variants: 78727026-C-T

27882529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron variant
orthologous variants: 78727012-A-G

27882529-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron variant
orthologous variants: 78727012-A-T

http://identifiers.org/hco/17/GRCh38#27882596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#78726955-C-A

27882596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: synonymous variant
orthologous variants: 78726955-C-T

27882619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: undefined
orthologous variants: 78726932-G-A

27882619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: missense variant
orthologous variants: 78726932-G-T

27882622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: undefined
orthologous variants: 78726929-G-A

27882622-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: missense variant
orthologous variants: 78726929-G-C

http://identifiers.org/hco/17/GRCh38#27882630-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#78726921-C-A

27882630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: missense variant
orthologous variants: 78726921-C-T

http://identifiers.org/hco/17/GRCh38#27882635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#78726916-C-A

27882635-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: missense variant
orthologous variants: 78726916-C-G

27882657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: missense variant
orthologous variants: 78726894-G-A

27882698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 78726855-T-C

27882732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron variant
orthologous variants: 78726822-A-G

27882757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron variant
orthologous variants: 78726797-A-G

27882819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron variant
orthologous variants: 78726738-G-T

http://identifiers.org/hco/17/GRCh38#27882825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#78726732-C-A

27882834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron variant
orthologous variants: 78726723-T-C

27882834-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron variant
orthologous variants: 78726723-T-G

http://identifiers.org/hco/17/GRCh38#27882906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#78726669-C-A

27882928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron variant
orthologous variants: 78726646-G-A

27882928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron variant
orthologous variants: 78726646-G-T

27882948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 78726626-C-T

http://identifiers.org/hco/17/GRCh38#27882949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#78726625-C-A

27882949-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 78726625-C-G

27882949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 78726625-C-T

27883042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 78726558-G-A

27883042-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 78726558-G-C

27883042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 78726558-G-T

27883102-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 78726506-C-G

27883102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 78726506-C-T

27883106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 78726502-G-A

27883106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 78726502-G-T

27883134-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant
orthologous variants: 78726474-G-C

27883134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant
orthologous variants: 78726474-G-T

27884641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron variant
orthologous variants: 78724026-A-G

27884773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron variant
orthologous variants: 78723881-G-A

27885056-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron variant
orthologous variants: 78723665-T-A

27885697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron variant
orthologous variants: 78723203-G-A

27885697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron variant
orthologous variants: 78723203-G-T

27885732-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron variant
orthologous variants: 78723168-T-A

27885732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron variant
orthologous variants: 78723168-T-C

27886210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron variant
orthologous variants: 78722676-A-G

27886210-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron variant
orthologous variants: 78722676-A-T

27886330-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron variant
orthologous variants: 78722556-A-T

27889722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron variant
orthologous variants: 78720242-G-A

27889810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron variant
orthologous variants: 78720185-C-T

27890004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron variant
orthologous variants: 78720035-T-C

27890588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron variant
orthologous variants: 78718937-G-A

27890857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron variant
orthologous variants: 78718677-C-T

27892578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78718105-G-A

27892921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78717807-T-C

http://identifiers.org/hco/17/GRCh38#27893053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#78717696-C-A

27893065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 78717681-C-T

27893099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78717648-T-C

27893147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78717608-G-A

27893153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78717602-A-G

27893156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78717599-G-A

27893156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78717599-G-T

27893172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 78717583-C-T

27893199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78717553-T-C

http://identifiers.org/hco/17/GRCh38#27893205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#78717547-C-A

http://identifiers.org/hco/17/GRCh38#27893241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#78717509-C-A

http://identifiers.org/hco/17/GRCh38#27893273-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#78717499-C-A

27893273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 78717499-C-T

27893376-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 78717400-C-G

http://identifiers.org/hco/17/GRCh38#27893397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#78717378-C-A

27893432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 78717350-G-A

27893432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 78717350-G-T

27893470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: non coding transcript exon variant
orthologous variants: 78717312-T-C

27893476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 78717306-A-G

http://identifiers.org/hco/17/GRCh38#27893506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#78717279-C-A

27893506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: non coding transcript exon variant
orthologous variants: 78717279-C-T

http://identifiers.org/hco/17/GRCh38#27893550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#78717264-C-A

http://identifiers.org/hco/17/GRCh38#27893793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#78717026-C-A

27893840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: non coding transcript exon variant
orthologous variants: 78716980-A-G

27894113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: non coding transcript exon variant
orthologous variants: 78716707-C-T

http://identifiers.org/hco/17/GRCh38#27894116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#78716704-C-A

27894149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: non coding transcript exon variant
orthologous variants: 78716668-C-T

27894267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: non coding transcript exon variant
orthologous variants: 78716558-G-T

27894368-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: non coding transcript exon variant
orthologous variants: 78716423-T-A

27894368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: non coding transcript exon variant
orthologous variants: 78716423-T-C

http://identifiers.org/hco/17/GRCh38#27894733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#78716075-C-A

27894733-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27314
most severe consequence: non coding transcript exon variant
orthologous variants: 78716075-C-G