171485649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 162567976-T-C

171485687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 162567941-G-A

171485687-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 162567941-G-T

171485706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 162567922-A-G

171485753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 162567874-G-T

171485899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162567782-C-T

171486282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162567522-A-G

171486373-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162567427-C-G

171486373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162567427-C-T

171486951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162566837-A-G

171487074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162566722-T-C

171487182-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162566612-T-A

171487951-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162565899-C-G

171487982-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162565869-G-C

171487982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162565869-G-T

http://identifiers.org/hco/1/GRCh38#171488100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#162565812-C-A

171488100-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162565812-C-G

171488103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162565809-C-T

171488429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162565247-A-G

171488778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162565008-G-T

171489064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162564700-T-C

171489124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162564645-A-G

171490559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162562876-G-T

171490756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162562696-A-G

171491435-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162561947-C-G

http://identifiers.org/hco/1/GRCh38#171492174-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#162560907-A-C

http://identifiers.org/hco/1/GRCh38#171492348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#162560834-C-A

http://identifiers.org/hco/1/GRCh38#171494334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#162559472-C-A

171494421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162559344-A-G

171495681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162557432-G-A

171513187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162550662-G-A

171513380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162550188-A-G

171513392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162550175-A-G

171513392-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162550175-A-T

171513407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162550158-A-G

171513599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162549942-G-A

171513985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162549609-A-G

171514046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162549550-A-G

http://identifiers.org/hco/1/GRCh38#171514432-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#162549201-A-C

171514492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162549149-A-G

171514492-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162549149-A-T

171514656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162548986-A-G

171514763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162548901-T-C

http://identifiers.org/hco/1/GRCh38#171514764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#162548900-C-A

171514764-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162548900-C-G

171514764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162548900-C-T

171514957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162548733-T-C

171515380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162548488-G-A

171515471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162548403-C-T

http://identifiers.org/hco/1/GRCh38#171515615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#162548291-C-A

http://identifiers.org/hco/1/GRCh38#171515618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#162548288-C-A

http://identifiers.org/hco/1/GRCh38#171515853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#162548054-C-A

171515860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 162548047-G-A

http://identifiers.org/hco/1/GRCh38#171515996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#162547947-C-A

171515996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162547947-C-T

171515998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162547945-G-A

171515998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162547945-G-T

171515999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162547944-G-A

171515999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162547944-G-T

171516000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162547943-T-C

171516521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162547267-G-A

171516842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162547036-T-C

171516862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162547016-A-G

171517236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162546773-T-C

171517347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162546681-G-A

171517485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162546573-T-C

171517519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162546545-A-G

171517520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162546544-T-C

171517531-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162546533-T-A

171517798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 162546273-C-T

171517849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162546221-G-A

171517899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162546184-A-G

171517899-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162546184-A-T

171517926-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162546157-T-A

171517926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162546157-T-C

http://identifiers.org/hco/1/GRCh38#171520738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#162544778-C-A

171520782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162544738-G-A

171520782-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162544738-G-C

171520782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162544738-G-T

171522159-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162543946-T-A

171522159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162543946-T-C

http://identifiers.org/hco/1/GRCh38#171522166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#162543939-C-A

171522166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162543939-C-T

171522399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162543763-T-C

171522788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162543585-A-G

171522801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162543572-G-T

171523089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162543417-C-T

http://identifiers.org/hco/1/GRCh38#171523124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#162543389-C-A

http://identifiers.org/hco/1/GRCh38#171523497-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#162542984-A-C

171523498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 162542983-G-A

171523514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 162542967-G-A

171523571-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162542910-A-T

171523614-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162542866-T-A

http://identifiers.org/hco/1/GRCh38#171524216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#162542738-C-A

171525282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162541450-T-C

171525341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162541395-A-G

171525439-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162541292-A-T

171527775-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162540940-T-A

171527775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162540940-T-C

171527775-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162540940-T-G

171527953-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162540763-T-G

http://identifiers.org/hco/1/GRCh38#171527958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#162540758-C-A

171527958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162540758-C-T

171527971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162540745-A-G

171528060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162540667-A-G

http://identifiers.org/hco/1/GRCh38#171528262-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#162540547-A-C

171528262-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162540547-A-T

171530677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162540028-G-A

171530710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162539995-C-T

171531039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162539764-A-G

171531850-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162539196-C-G

171532021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162539031-C-T

171532490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 162538249-C-T

171532532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 162538207-G-A

171532532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 162538207-G-T

171532658-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 162538087-G-C

http://identifiers.org/hco/1/GRCh38#171535406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#162537275-C-A

171535406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162537275-C-T

171535437-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: missense variant
orthologous variants: 162537244-C-G

171535437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: missense variant
orthologous variants: 162537244-C-T

171535768-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162536905-A-T

171535771-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162536901-C-G

171535771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162536901-C-T

http://identifiers.org/hco/1/GRCh38#171536472-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#162536232-A-C

171536915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162535733-A-G

171537358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: missense variant
orthologous variants: 162535445-G-A

171537358-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: missense variant
orthologous variants: 162535445-G-C

171537358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: missense variant
orthologous variants: 162535445-G-T

171537478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162535328-T-C

171537478-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162535328-T-G

171537483-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162535323-T-A

171539607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162534511-T-C

171539856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162534322-T-C

171539856-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162534322-T-G

http://identifiers.org/hco/1/GRCh38#171539907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#162534252-C-A

171540053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: missense variant
orthologous variants: 162534106-G-A

171540212-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: missense variant
orthologous variants: 162533947-G-C

171540659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: missense variant
orthologous variants: 162533503-C-T

171540929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: missense variant
orthologous variants: 162533236-C-T

171541400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: missense variant
orthologous variants: 162532765-C-T

171541418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: missense variant
orthologous variants: 162532747-A-G

http://identifiers.org/hco/1/GRCh38#171541463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#162532702-C-A

171541753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: synonymous variant
orthologous variants: 162532412-A-G

171542026-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: missense variant
orthologous variants: 162532142-C-G

171542026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: synonymous variant
orthologous variants: 162532142-C-T

171542036-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: missense variant
orthologous variants: 162532132-C-G

171542512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162531751-G-T

171544850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162530538-A-G

171545231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162530174-G-A

171545327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162530087-C-T

171545340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162530074-T-C

171545681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: missense variant
orthologous variants: 162529755-T-C

171545994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162529503-T-C

171546228-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162529301-T-A

171546420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162529150-A-G

171550324-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162526366-T-A

171557393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: missense variant
orthologous variants: 162525729-T-C

171557408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: missense variant
orthologous variants: 162525714-G-A

171557408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: missense variant
orthologous variants: 162525714-G-T

http://identifiers.org/hco/1/GRCh38#171557425-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#162525697-A-C

171557425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: synonymous variant
orthologous variants: 162525697-A-G

171557425-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: synonymous variant
orthologous variants: 162525697-A-T

171557446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: synonymous variant
orthologous variants: 162525673-A-G

171557470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: synonymous variant
orthologous variants: 162525649-G-A

171557483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: missense variant
orthologous variants: 162525630-A-G

171557516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: missense variant
orthologous variants: 162525597-C-T

http://identifiers.org/hco/1/GRCh38#171557643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#162525476-C-A

171557643-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: missense variant
orthologous variants: 162525476-C-G

171557690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: missense variant
orthologous variants: 162525429-T-C

171557690-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: missense variant
orthologous variants: 162525429-T-G

171557745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: missense variant
orthologous variants: 162525374-C-T

http://identifiers.org/hco/1/GRCh38#171557825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#162525294-C-A

171557825-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: missense variant
orthologous variants: 162525294-C-G

http://identifiers.org/hco/1/GRCh38#171557864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#162525255-C-A

171557864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: missense variant
orthologous variants: 162525255-C-T

171558081-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: missense variant
orthologous variants: 162525062-C-G

171558110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: missense variant
orthologous variants: 162525033-C-T

171558139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: synonymous variant
orthologous variants: 162525004-G-A

171558159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162524983-G-T

171558165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162524977-A-G

171558165-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162524977-A-T

171558169-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162524973-G-C

171558169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162524973-G-T

171561901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162523410-C-T

http://identifiers.org/hco/1/GRCh38#171566188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#162520541-C-A

171566188-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162520541-C-G

171566188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162520541-C-T

171566199-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162520527-T-A

171566691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: missense_variant, undefined
orthologous variants: 162520092-G-A

171566691-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: missense_variant, undefined
orthologous variants: 162520092-G-C

171566739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: missense variant
orthologous variants: 162520044-A-G

171566775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: missense variant
orthologous variants: 162520008-T-C

171566980-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162519668-T-A

171567774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162518957-C-T

171567775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162518956-G-A

171567855-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162518878-T-G

171568262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, missense_variant
orthologous variants: 162518785-T-C

171568408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162518646-T-C

http://identifiers.org/hco/1/GRCh38#171568432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#162518627-C-A

171568432-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162518627-C-G

http://identifiers.org/hco/1/GRCh38#171568442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#162518617-C-A

171568632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162518407-G-A

171568708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162518333-A-G

171568733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162518300-A-G

171569570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162517515-G-T

171569670-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162517479-T-G

171569743-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162517421-T-A

171570038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162517213-T-C

171570049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162517202-G-A

171570271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162517004-G-A

171570297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162516977-G-A

171570464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162516494-G-A

171570623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162516293-A-G

171571071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162515963-G-A

171571099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162515936-C-T

171571103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162515932-T-C

171571320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 162515784-G-A

171571320-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 162515784-G-C

171571365-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, missense_variant
orthologous variants: 162515739-C-G

http://identifiers.org/hco/1/GRCh38#171571485-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#162515620-A-C

171571651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162515373-T-C

171571785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162515251-C-T

171571870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162515175-A-G

http://identifiers.org/hco/1/GRCh38#171572573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#162514609-C-A

171572858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162514349-T-C

171572934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162514283-C-T

171573004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162514194-A-G

171573562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162513488-T-C

171573583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162513467-T-C

171573649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162513389-A-G

171574847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162511909-A-G

171574975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: missense variant
orthologous variants: 162511775-A-G

171574999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: missense variant
orthologous variants: 162511751-G-A

171574999-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: missense variant
orthologous variants: 162511751-G-C

http://identifiers.org/hco/1/GRCh38#171575041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#162511709-C-A

171575074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: missense variant
orthologous variants: 162511676-G-A

171575122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: synonymous variant
orthologous variants: 162511628-C-T

171575132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162511618-G-T

http://identifiers.org/hco/1/GRCh38#171577553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#162509969-C-A

171577553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: missense variant
orthologous variants: 162509969-C-T

171577641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162509881-A-G

171577706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162509823-T-C

http://identifiers.org/hco/1/GRCh38#171577715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#162509816-C-A

171577715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162509816-C-T

171578967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162509261-A-G

171578967-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162509261-A-T

171579359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: missense variant
orthologous variants: 162508895-A-G

171579509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162508760-A-G

171579565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162508707-A-G

171579731-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162508569-T-A

171579731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162508569-T-C

171579731-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162508569-T-G

171579984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162508306-T-C

http://identifiers.org/hco/1/GRCh38#171582343-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#162507777-A-C

171582343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162507777-A-G

171584590-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162507000-T-A

171584650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162506946-T-C

171586971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162505828-A-G

171587132-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: missense variant
orthologous variants: 162505666-A-T

171587227-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162505571-T-A

171587253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162505496-G-T

http://identifiers.org/hco/1/GRCh38#171587328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#162505302-C-A

171587875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162504796-T-C

171588067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162504666-G-A

171588079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162504657-C-T

171588112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162504620-A-G

171588580-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162504181-C-G

171588596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162504164-A-G

171588602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162504158-T-C

171588683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162504101-T-C

171588717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162504067-A-G

171589045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162503756-G-T

171589831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162502950-A-G

171589831-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162502950-A-T

171589902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162502878-G-A

http://identifiers.org/hco/1/GRCh38#171589983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#162502797-C-A

171589983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162502797-C-T

http://identifiers.org/hco/1/GRCh38#171590021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#162502775-C-A

171590021-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162502775-C-G

171590021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162502775-C-T

171590383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162502448-C-T

171590426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162502408-T-C

171590561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162502291-T-C

171591050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 162501816-A-G

171591358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162501450-G-A

171591358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162501450-G-T

http://identifiers.org/hco/1/GRCh38#171591404-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#162501401-A-C

171591404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162501401-A-G

171591404-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: intron variant
orthologous variants: 162501401-A-T

http://identifiers.org/hco/1/GRCh38#171591922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#162500905-C-A

171591922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: 3 prime UTR variant
orthologous variants: 162500905-C-T

171591924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: 3 prime UTR variant
orthologous variants: 162500903-A-G

http://identifiers.org/hco/1/GRCh38#171591997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#162500844-C-A

http://identifiers.org/hco/1/GRCh38#171592051-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#162500799-A-C

171592051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: 3 prime UTR variant
orthologous variants: 162500799-A-G

171592051-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: 3 prime UTR variant
orthologous variants: 162500799-A-T

http://identifiers.org/hco/1/GRCh38#171592056-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#162500794-A-C

171592056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: 3 prime UTR variant
orthologous variants: 162500794-A-G

171592056-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: 3 prime UTR variant
orthologous variants: 162500794-A-T

http://identifiers.org/hco/1/GRCh38#171592109-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#162500760-A-C

171592109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: 3 prime UTR variant
orthologous variants: 162500760-A-G

171592109-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: 3 prime UTR variant
orthologous variants: 162500760-A-T

http://identifiers.org/hco/1/GRCh38#171592196-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#162500687-A-C

171592231-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: 3 prime UTR variant
orthologous variants: 162500650-A-T

171592275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: 3 prime UTR variant
orthologous variants: 162500607-T-C

171592578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: 3 prime UTR variant
orthologous variants: 162500307-G-A

171592578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: 3 prime UTR variant
orthologous variants: 162500307-G-T

171592696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: 3 prime UTR variant
orthologous variants: 162500195-G-T

171592773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: 3 prime UTR variant
orthologous variants: 162500110-C-T

http://identifiers.org/hco/1/GRCh38#171592791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#162500092-C-A

171592791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: 3 prime UTR variant
orthologous variants: 162500092-C-T

171592838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: 3 prime UTR variant
orthologous variants: 162500045-G-A

171592847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: 3 prime UTR variant
orthologous variants: 162500036-T-C

171592851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: 3 prime UTR variant
orthologous variants: 162500032-A-G

171592898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: 3 prime UTR variant
orthologous variants: 162499985-G-T

171593067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: 3 prime UTR variant
orthologous variants: 162499800-G-A

171593071-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: 3 prime UTR variant
orthologous variants: 162499796-C-G

171593110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: 3 prime UTR variant
orthologous variants: 162499757-G-A

171593144-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: 3 prime UTR variant
orthologous variants: 162499720-T-A

171593153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: 3 prime UTR variant
orthologous variants: 162499711-G-T

171593236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: 3 prime UTR variant
orthologous variants: 162499625-C-T

171593257-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: 3 prime UTR variant
orthologous variants: 162499604-T-A

171593331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: 3 prime UTR variant
orthologous variants: 162499535-A-G

171593425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: 3 prime UTR variant
orthologous variants: 162499438-C-T

http://identifiers.org/hco/1/GRCh38#171593449-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#162499414-A-C

171593449-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: 3 prime UTR variant
orthologous variants: 162499414-A-T

171593453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: 3 prime UTR variant
orthologous variants: 162499410-A-G

http://identifiers.org/hco/1/GRCh38#171593486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24903
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#162499377-C-A