97366751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139457987-T-C

97366912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139457839-G-A

97366912-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139457839-G-C

97366912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139457839-G-T

97366978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139457776-G-T

97367033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139457721-G-T

97367074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139457684-G-A

97367272-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139457526-G-C

97367284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139457514-C-T

97367501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139457298-T-C

97367631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139457161-G-A

97367631-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139457161-G-C

97367663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139457129-G-A

97367681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139457111-G-T

97367683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139457109-C-T

97367729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139457066-C-T

97367882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139456918-A-G

97367893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139456907-T-C

97367978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139456839-T-C

97367981-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139456836-A-T

97368290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139456543-T-C

97368376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139456475-A-G

http://identifiers.org/hco/4/GRCh38#97368391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#139456464-C-A

97368391-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139456464-C-G

97368393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139456462-A-G

http://identifiers.org/hco/4/GRCh38#97371765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#139454708-C-A

97371765-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139454708-C-G

97371767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139454706-A-G

97371769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139454704-T-C

97371793-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139454672-T-G

97375682-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139449555-A-T

97375873-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139449367-G-C

97376322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139448719-G-A

97376330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139448711-G-T

97376363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139448651-A-G

97376390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139448606-T-C

97376426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139448529-T-C

97376496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139448464-T-C

97376698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139448290-T-C

97376807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139448189-C-T

97376863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139448140-T-C

97378490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139446931-G-A

97378510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139446902-G-A

97378510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139446902-G-T

http://identifiers.org/hco/4/GRCh38#97378639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#139446802-C-A

97378639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139446802-C-T

97378732-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139446712-T-G

97378953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139446490-T-C

97378965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139446483-T-C

97379020-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139446428-T-A

97379020-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139446428-T-G

97379060-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139446389-T-A

97379198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139446249-A-G

97379401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139446054-T-C

97379493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139445956-C-T

97385090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139445715-G-A

97385162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139445658-G-A

97385166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139445654-G-A

97385178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139445642-T-C

97385251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139445571-T-C

97385293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139445528-T-C

97385878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139444974-T-C

97385878-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139444974-T-G

97386076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139444811-T-C

97386098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139444792-G-A

97386098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139444792-G-T

97386120-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139444780-A-T

97386179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139444719-A-G

97386228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139444669-C-T

97386284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139444607-G-T

97386351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139444540-C-T

97386361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139444525-C-T

97386507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139444383-C-T

97386636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139444257-T-C

97386813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139444088-G-T

97387094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139443807-C-T

97387491-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139443239-T-G

97387517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139443215-C-T

97387558-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139443184-A-T

http://identifiers.org/hco/4/GRCh38#97387671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#139443092-C-A

http://identifiers.org/hco/4/GRCh38#97387684-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#139443079-A-C

97387692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139443071-A-G

http://identifiers.org/hco/4/GRCh38#97387778-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#139442986-A-C

97387826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139442943-G-T

97391708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139440520-T-C

97391814-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139440419-A-T

97392020-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139440210-G-C

97392021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139440209-C-T

97392053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139440178-T-C

97392345-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139439900-T-A

97392345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139439900-T-C

97392384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139439861-G-A

97392406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139439838-A-G

97392623-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139439622-T-A

97392659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139439586-T-C

97392723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139439526-T-C

97392727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 139439522-G-A

97392727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 139439522-G-T

http://identifiers.org/hco/4/GRCh38#97392745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#139439504-C-A

97392820-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139439418-A-T

97392982-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139439254-G-C

97393135-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139439102-T-G

http://identifiers.org/hco/4/GRCh38#97393425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#139438867-C-A

http://identifiers.org/hco/4/GRCh38#97393608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#139438700-C-A

97393721-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139438601-C-G

97394031-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139438248-G-C

97394486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139437333-C-T

97394596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139437209-G-A

97394842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139436993-T-C

97395143-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139436239-T-A

97395146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139436232-C-T

97395267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139436108-T-C

97395326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139436046-A-G

97395350-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139436023-T-A

97395528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139435837-C-T

97396458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139435131-G-A

97396576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139435014-G-A

97396584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139435006-G-T

97397035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139434567-C-T

97397202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139434398-T-C

97404493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139431659-A-G

97404772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139431358-A-G

97410960-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139427407-T-G

97411018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139427355-G-A

97411121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139427259-T-C

97411273-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139427118-A-T

97411300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139427091-C-T

97411720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139426683-C-T

97411734-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139426669-G-C

http://identifiers.org/hco/4/GRCh38#97411757-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#139426646-A-C

97411831-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139426573-G-C

97412024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139426384-C-T

http://identifiers.org/hco/4/GRCh38#97412051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#139426362-C-A

97412067-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139426346-T-A

97412285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139426134-A-G

97412379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139426042-C-T

97412634-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139425809-G-C

97412735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139425712-C-T

97412744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139425703-A-G

97412891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139425559-C-T

97412970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139425487-A-G

97417067-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139419929-G-C

97417126-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139419871-T-A

http://identifiers.org/hco/4/GRCh38#97417156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#139419847-C-A

http://identifiers.org/hco/4/GRCh38#97417200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#139419809-C-A

97417200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139419809-C-T

97417229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139419780-T-C

97417313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139419700-C-T

97417391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139419620-C-T

97420252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139419418-A-G

http://identifiers.org/hco/4/GRCh38#97420333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#139419340-C-A

97420333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139419340-C-T

97421347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139418930-T-C

97421461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139418840-T-C

97439989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139418183-T-C

97440007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139418201-A-G

97440184-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139418377-T-G

97440189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139418382-T-C

97440220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139418413-T-C

97440247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139418440-T-C

97440345-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139418536-A-T

http://identifiers.org/hco/4/GRCh38#97440347-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#139418538-A-C

97440400-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139418168-T-G

http://identifiers.org/hco/4/GRCh38#97440427-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#139418142-A-C

97440427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139418142-A-G

97440600-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139417968-G-C

97440779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139417780-A-G

97441772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139414692-G-T

97441978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139414483-T-C

97442025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139414410-C-T

http://identifiers.org/hco/4/GRCh38#97442036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#139414399-C-A

97442045-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139414390-A-T

97442358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139414118-C-T

97442474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139413990-T-C

97442483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139413981-T-C

http://identifiers.org/hco/4/GRCh38#97445501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#139408366-C-A

97445536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139408339-C-T

97445823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139408164-A-G

97445926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139408072-A-G

97446022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139407980-T-C

97446124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139407881-T-C

97449296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139407041-C-T

97449339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139407013-G-A

97453927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139405785-G-T

97453936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139405776-T-C

97454110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139405607-A-G

97457857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139404977-A-G

97457880-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139404954-T-A

http://identifiers.org/hco/4/GRCh38#97457881-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#139404953-A-C

97457902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139404932-G-A

97457911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139404923-G-T

http://identifiers.org/hco/4/GRCh38#97457978-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#139404862-A-C

97457978-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139404862-A-T

97458023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139404839-G-A

97458048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139404814-G-A

97458067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139404797-T-C

97458222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139404641-G-A

http://identifiers.org/hco/4/GRCh38#97458250-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#139404613-A-C

97458288-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139404574-T-A

97458311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139404551-A-G

97458671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139404190-A-G

97458691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139404173-C-T

97458740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139404122-G-T

97459241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139403667-A-G

97465924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139396709-T-C

97465940-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139396693-T-G

97466218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139396400-C-T

97466228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139396391-A-G

97466541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139395468-G-A

97466852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139394907-A-G

97466953-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139394808-C-G

97466953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139394808-C-T

97467272-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139394481-A-T

97467308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139394447-T-C

97467605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139394160-A-G

97467682-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139394090-A-T

97467983-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139393779-T-A

97468025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139393740-A-G

97468236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139393534-G-A

97468341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139393428-A-G

97468396-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139393385-A-T

97468469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139393331-G-A

97468710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139393123-C-T