128809714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 41517853-A-G

128809714-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 41517853-A-T

128809768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: 5 prime UTR variant
orthologous variants: 41517904-C-T

128809783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 41517919-G-A

128809783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 41517919-G-T

http://identifiers.org/hco/4/GRCh38#128809793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#41517929-C-A

128809793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 41517929-C-T

128810262-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41518322-G-T

http://identifiers.org/hco/4/GRCh38#128810483-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#41518509-A-C

128810483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron variant
orthologous variants: 41518509-A-G

128811257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron variant
orthologous variants: 41519300-G-A

128811257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron variant
orthologous variants: 41519300-G-T

http://identifiers.org/hco/4/GRCh38#128811542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#41519582-C-A

128811542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41519582-C-T

128811630-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41519666-G-C

128812132-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41520068-T-G

128812330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41520214-G-A

http://identifiers.org/hco/4/GRCh38#128812373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#41520251-C-A

128812373-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 41520251-C-G

128812373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 41520251-C-T

128812471-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41520383-C-G

128812524-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41520458-G-C

128812826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41520821-C-T

128812856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 41520852-T-C

128813390-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41521283-T-G

128813396-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41521286-A-T

128815431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41522410-C-T

128815715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41522687-C-T

128815879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41522843-A-G

http://identifiers.org/hco/4/GRCh38#128816004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#41522947-C-A

http://identifiers.org/hco/4/GRCh38#128816071-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#41523019-A-C

128816209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41523711-A-G

128816513-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41523957-A-T

128816585-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41524024-C-G

128816724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41524255-G-A

128816853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41524495-G-T

128817755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41524868-T-C

128817844-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41524950-C-G

128817925-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41525014-A-T

128818030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41525107-T-C

128818635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41525377-C-T

128820461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41526508-A-G

128820686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41526709-C-T

128821084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41527039-G-A

128821173-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41527110-A-T

128822768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41527397-A-G

128822830-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41527462-T-A

128822884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41527511-G-T

128823156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41527786-G-A

128823205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41527951-G-A

128823236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41527978-A-G

128823283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41528022-T-C

128823301-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41528040-T-A

128823497-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41528231-A-T

http://identifiers.org/hco/4/GRCh38#128824542-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#41528832-A-C

128824542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41528832-A-G

128824594-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41528883-T-G

128824648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41528931-G-A

128824652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41528935-A-G

128824720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41529008-G-A

128825687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41529526-C-T

128825713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41529552-A-G

128825738-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41529573-T-A

128825754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41529589-A-G

128825760-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41529595-G-C

http://identifiers.org/hco/4/GRCh38#128826074-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#41529809-A-C

128827486-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41531238-C-G

128827676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41531396-T-C

128828046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41532242-A-G

128828618-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41532767-T-A

128828673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41532812-A-G

http://identifiers.org/hco/4/GRCh38#128828868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#41532976-C-A

128828868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41532976-C-T

http://identifiers.org/hco/4/GRCh38#128830636-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#41534651-A-C

128830848-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41534849-C-G

128831148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41535055-T-C

128831153-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41535060-G-C

128831361-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41535284-T-A

128831422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41535329-G-A

128831422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41535329-G-T

128831428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41535335-A-G

128831515-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 41535415-A-T

http://identifiers.org/hco/4/GRCh38#128831531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#41535432-C-A

128831531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 41535432-C-T

128831691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41535588-G-A

http://identifiers.org/hco/4/GRCh38#128831843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#41535740-C-A

128831843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41535740-C-T

128831875-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41535772-T-G

128832112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41536008-G-A

128832203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41536105-G-T

128832275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41536159-T-C

128832489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41536356-T-C

128832790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41536656-T-C

128835227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41537771-G-T

128835337-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41537887-C-G

128835394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41537932-T-C

128835537-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41538035-G-C

128835537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41538035-G-T

128835759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41538204-G-A

128835847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41538299-A-G

128835899-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41538351-T-A

http://identifiers.org/hco/4/GRCh38#128836117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#41538563-C-A

128838350-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41539648-T-A

128838356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41539654-T-C

128838444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41539727-A-G

128838605-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41539953-A-T

128838650-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41539983-T-A

128838669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41540000-T-C

128838709-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41540026-A-T

128838783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41540199-C-T

128838906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41540341-C-T

128838992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41540417-G-A

http://identifiers.org/hco/4/GRCh38#128839078-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#41540513-A-C

128839103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41540542-A-G

128839638-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41540988-G-C

http://identifiers.org/hco/4/GRCh38#128839654-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#41541004-A-C

128839654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41541004-A-G

128839654-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41541004-A-T

128841018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41541814-A-G

128841108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41541880-T-C

128841296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41542051-T-C

128841547-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41542312-T-A

128841547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41542312-T-C

128843005-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 41543424-C-G

128843005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 41543424-C-T

128843108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41543538-T-C

128843244-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41543653-T-G

128843462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41543857-G-A

128843462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41543857-G-T

128843511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41543901-A-G

128843667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41544068-T-C

128843883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41544252-T-C

128844733-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41544900-T-G

128844796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41544960-A-G

128844862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41545025-C-T

128844951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41545087-A-G

128845053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41545190-G-T

128845089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41545204-G-A

128845240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41545347-C-T

128845307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41545396-T-C

128846132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41545890-C-T

http://identifiers.org/hco/4/GRCh38#128846224-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#41545974-C-A

128846224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41545974-C-T

128846231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41545981-A-G

128846299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41546051-G-A

128846299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41546051-G-T

128846370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 41546113-T-C

128846370-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 41546113-T-G

128846538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41546281-G-A

http://identifiers.org/hco/4/GRCh38#128846602-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#41546330-A-C

128846735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41546427-C-T

128846832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41546514-G-A

128846855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41546530-C-T

128846944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41546603-G-A

128846978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41546621-C-T

http://identifiers.org/hco/4/GRCh38#128847134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#41546735-C-A

128847134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41546735-C-T

128847693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41547139-G-A

128847878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41547305-T-C

128848050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41547466-G-A

128848347-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41547768-T-G

128848835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41548063-T-C

128849058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 41548280-G-A

http://identifiers.org/hco/4/GRCh38#128849201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#41548412-C-A

128849229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41548440-G-T

128849230-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41548441-T-G

128849376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41548615-C-T

128849861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41548993-G-T

128850710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41549438-T-C

128850713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41549441-A-G

http://identifiers.org/hco/4/GRCh38#128850717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#41549444-C-A

128851402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41550758-G-A

http://identifiers.org/hco/4/GRCh38#128851408-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#41550764-A-C

128851969-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41550966-T-A

128852003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41550998-A-G

128852032-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41551027-G-C

128852032-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41551027-G-T

128852226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: synonymous variant
orthologous variants: 41551219-T-C

128852226-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: missense variant
orthologous variants: 41551219-T-G

http://identifiers.org/hco/4/GRCh38#128852346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#41551344-C-A

128852694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron variant
orthologous variants: 41551524-G-T

128852827-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron variant
orthologous variants: 41551596-T-A

128852850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron variant
orthologous variants: 41551611-C-T

128852858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron variant
orthologous variants: 41551619-C-T

128853605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron variant
orthologous variants: 41552472-G-A

128853657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron variant
orthologous variants: 41552523-G-T

128853797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron variant
orthologous variants: 41552751-A-G

128853905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron variant
orthologous variants: 41552851-G-A

http://identifiers.org/hco/4/GRCh38#128853940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#41552875-C-A

128853956-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron variant
orthologous variants: 41552887-G-C

128854139-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron variant
orthologous variants: 41553017-A-T

128854307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron variant
orthologous variants: 41553148-C-T

128854397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron variant
orthologous variants: 41553225-T-C

128854397-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron variant
orthologous variants: 41553225-T-G

128854536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron variant
orthologous variants: 41553348-C-T

128854578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron variant
orthologous variants: 41553390-A-G

128854593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron variant
orthologous variants: 41553405-G-A

128854593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron variant
orthologous variants: 41553405-G-T

128854790-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron variant
orthologous variants: 41553594-T-G

128854992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron variant
orthologous variants: 41553742-A-G

128854992-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron variant
orthologous variants: 41553742-A-T

128855265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron variant
orthologous variants: 41553966-C-T

128855308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron variant
orthologous variants: 41554009-C-T

128855329-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron variant
orthologous variants: 41554028-T-G

128855394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron variant
orthologous variants: 41554089-G-T

http://identifiers.org/hco/4/GRCh38#128855498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#41554169-C-A

128855498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron variant
orthologous variants: 41554169-C-T

http://identifiers.org/hco/4/GRCh38#128855656-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#41554483-A-C

128856178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron variant
orthologous variants: 41554686-T-C

128856471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron variant
orthologous variants: 41554920-C-T

128856830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron variant
orthologous variants: 41555233-A-G

128856984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron variant
orthologous variants: 41555343-C-T

128857513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron variant
orthologous variants: 41555979-G-T

128857521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron variant
orthologous variants: 41555989-G-T

128857548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron variant
orthologous variants: 41556011-G-T

128857904-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron variant
orthologous variants: 41556251-T-G

http://identifiers.org/hco/4/GRCh38#128858725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#41556844-C-A

128858855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron variant
orthologous variants: 41556946-A-G

128858885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron variant
orthologous variants: 41556975-G-T

128859209-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron variant
orthologous variants: 41557250-G-C

128859209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron variant
orthologous variants: 41557250-G-T

128859722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron variant
orthologous variants: 41557287-T-C

128860301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron variant
orthologous variants: 41557849-G-A

128860315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron variant
orthologous variants: 41557863-T-C

128860471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron variant
orthologous variants: 41557987-A-G

128861263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron variant
orthologous variants: 41558662-G-A

128861317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron variant
orthologous variants: 41558718-C-T

128861630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron variant
orthologous variants: 41558845-C-T

128861641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron variant
orthologous variants: 41558856-A-G

128861982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: synonymous variant
orthologous variants: 41559183-G-A

128862134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: missense variant
orthologous variants: 41559335-A-G

http://identifiers.org/hco/4/GRCh38#128862344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#41559538-C-A

128862344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 41559538-C-T

http://identifiers.org/hco/4/GRCh38#128862465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#41559637-C-A

128862465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 41559637-C-T

http://identifiers.org/hco/4/GRCh38#128862521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#41559691-C-A

128862521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 41559691-C-T

128862643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 41559813-G-A

128862643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 41559813-G-T

128862706-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 41559878-G-T

128862807-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 41559978-G-C

128862807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 41559978-G-T

http://identifiers.org/hco/4/GRCh38#128862845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#41560005-C-A

128862845-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 41560005-C-G

128862939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 41560099-T-C

128862939-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 41560099-T-G

128863108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 41560270-C-T

http://identifiers.org/hco/4/GRCh38#128863164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#41560326-C-A

128863164-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 41560326-C-G

128863164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 41560326-C-T

128863292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 41560451-A-G

http://identifiers.org/hco/4/GRCh38#128863298-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#41560457-A-C

128863298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 41560457-A-G

http://identifiers.org/hco/4/GRCh38#128863524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#41560780-C-A

128863524-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 41560780-C-G

128863532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 41560788-A-G

128863541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 41560797-A-G

128863666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 41560910-C-T

128863966-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 41561173-T-A

128863979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 41561186-C-T

128864107-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 41561328-T-G

128864122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 41561343-A-G

128864507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 41561423-T-C

128864708-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron variant
orthologous variants: 41561626-T-A

128864708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron variant
orthologous variants: 41561626-T-C

128864708-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron variant
orthologous variants: 41561626-T-G

http://identifiers.org/hco/4/GRCh38#128865101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#41561973-C-A

128865101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron_variant, undefined
orthologous variants: 41561973-C-T

http://identifiers.org/hco/4/GRCh38#128865176-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#41562054-C-A

128865179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron_variant, undefined
orthologous variants: 41562057-G-A

128865179-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron_variant, undefined
orthologous variants: 41562057-G-C

128865324-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron_variant, undefined
orthologous variants: 41562196-G-C

128866049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron_variant, undefined
orthologous variants: 41562778-C-T

http://identifiers.org/hco/4/GRCh38#128866099-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#41562816-A-C

128866562-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron_variant, undefined
orthologous variants: 41563183-C-G

128866820-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron_variant, undefined
orthologous variants: 41563357-T-A

128866933-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron_variant, undefined
orthologous variants: 41563427-G-C

128866933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron_variant, undefined
orthologous variants: 41563427-G-T

128867261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron_variant, undefined
orthologous variants: 41563753-G-A

http://identifiers.org/hco/4/GRCh38#128867755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#41564139-C-A

128867935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 41564317-A-G

128868057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron_variant, undefined
orthologous variants: 41564433-T-C

128868057-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron_variant, undefined
orthologous variants: 41564433-T-G

128868069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron_variant, undefined
orthologous variants: 41564445-A-G

128868105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron_variant, undefined
orthologous variants: 41564481-G-A

128868105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron_variant, undefined
orthologous variants: 41564481-G-T

http://identifiers.org/hco/4/GRCh38#128868111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#41564487-C-A

128868215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron_variant, undefined
orthologous variants: 41564589-T-C

128868432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron_variant, undefined
orthologous variants: 41564802-C-T

128868584-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron_variant, undefined
orthologous variants: 41564945-C-G

128868770-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron_variant, undefined
orthologous variants: 41565109-A-T

128868879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron_variant, undefined
orthologous variants: 41565197-A-G

128869241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron_variant, undefined
orthologous variants: 41565459-G-A

128869241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron_variant, undefined
orthologous variants: 41565459-G-T

128869579-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron_variant, undefined
orthologous variants: 41565674-A-T

http://identifiers.org/hco/4/GRCh38#128869597-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#41565693-A-C

128869693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron_variant, undefined
orthologous variants: 41565773-A-G

128869760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron_variant, undefined
orthologous variants: 41565985-G-A

128870176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron_variant, undefined
orthologous variants: 41566368-A-G

128870179-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron_variant, undefined
orthologous variants: 41566371-G-C

128870331-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron_variant, undefined
orthologous variants: 41566480-C-G

128870731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron_variant, undefined
orthologous variants: 41567074-A-G

128870792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: intron_variant, undefined
orthologous variants: 41567122-G-A

128871131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 41567356-G-A

128871147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 41567382-C-T

128871150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 41567385-A-G

http://identifiers.org/hco/4/GRCh38#128871329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#41567537-C-A

128871329-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 41567537-C-G

128871452-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 41567652-G-C

128871521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 41567721-G-A

128871539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 41567739-T-C

128872108-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 41568284-G-C

128872232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant, undefined
orthologous variants: 41568408-C-T

128872331-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 41568500-G-T

128872335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 41568504-A-G

http://identifiers.org/hco/4/GRCh38#128872340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#41568509-C-A

128872542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 41568715-T-C

128872543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 41568716-A-G

128872650-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 41568839-T-A

128872757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 41568930-A-G

128872781-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 41568947-T-A

128872781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 41568947-T-C

128872868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 41569026-A-G

128872989-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 41569136-G-C

128873755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 41569824-T-C

128874079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 41570135-G-T

http://identifiers.org/hco/4/GRCh38#128874178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#41570232-C-A

128874178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 41570232-C-T

128874423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 41570476-T-C

128874505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30027
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 41570565-T-C