33180410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 151028572-C-T

33180629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151028789-G-T

33180677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151028839-G-A

33180677-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151028839-G-C

33180928-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151029096-T-A

33180942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151029112-G-A

33181063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151029269-C-T

33181251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151029478-G-A

33181449-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151029845-T-A

33181541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151029970-A-G

33184588-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151030615-C-G

33184638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151030665-T-C

33184685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151030708-G-A

33184739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151030760-G-A

http://identifiers.org/hco/13/GRCh38#33185175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#151031394-C-A

33185272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151031490-G-A

33185351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151031580-A-G

33185352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151031581-C-T

33185359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151031588-T-C

33185422-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151031645-A-T

http://identifiers.org/hco/13/GRCh38#33185480-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#151031691-A-C

33185570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151031770-T-C

33185595-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151031797-T-A

http://identifiers.org/hco/13/GRCh38#33185848-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#151032005-A-C

http://identifiers.org/hco/13/GRCh38#33185854-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#151032011-A-C

33185854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151032011-A-G

33185904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 151032056-C-T

33185938-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 151032081-T-A

33185938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 151032081-T-C

33185938-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 151032081-T-G

33186011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 151032157-G-A

33186011-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 151032157-G-C

33186012-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 151032158-G-C

33186016-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 151032162-C-G

33186024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 151032170-G-A

33186024-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 151032170-G-C

33186024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 151032170-G-T

33186064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 151032208-C-T

http://identifiers.org/hco/13/GRCh38#33186106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#151032253-C-A

33186106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151032253-C-T

33186108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151032255-G-A

33186108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151032255-G-T

http://identifiers.org/hco/13/GRCh38#33186114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#151032261-C-A

33186114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151032261-C-T

http://identifiers.org/hco/13/GRCh38#33186124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#151032271-C-A

33186124-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151032271-C-G

33186124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151032271-C-T

http://identifiers.org/hco/13/GRCh38#33186195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#151032342-C-A

33186195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151032342-C-T

http://identifiers.org/hco/13/GRCh38#33186216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#151032363-C-A

33186399-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151032534-T-G

33187002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151033324-C-T

33187024-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151033346-A-T

33188234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 151033719-G-T

33188241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 151033723-T-C

http://identifiers.org/hco/13/GRCh38#33188325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#151033815-C-A

33188697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151034178-T-C

33188924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151034414-G-A

33190013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151035290-T-C

33191033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151035645-G-T

33191314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151035983-G-T

33191763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151036444-C-T

33191872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151036552-T-C

33192114-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151036781-T-A

33192114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151036781-T-C

33192287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151036938-C-T

33193103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151037340-G-T

33193550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151037776-A-G

http://identifiers.org/hco/13/GRCh38#33193741-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#151037948-C-A

33194118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151038327-T-C

33194309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151038544-G-A

33194543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151039040-A-G

http://identifiers.org/hco/13/GRCh38#33194570-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#151039067-A-C

33194570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151039067-A-G

http://identifiers.org/hco/13/GRCh38#33194631-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#151039126-A-C

http://identifiers.org/hco/13/GRCh38#33194776-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#151039273-A-C

33194898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151039387-T-C

33194921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151039410-A-G

33195192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151039691-T-C

33195218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151039709-G-T

33195478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 151040050-G-T

http://identifiers.org/hco/13/GRCh38#33195571-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#151040143-A-C

33195571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 151040143-A-G

33197521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151041843-A-G

33197629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151041947-G-A

33197667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151041981-T-C

33197750-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151042069-T-A

33198661-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151042102-A-T

33198811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151042233-C-T

33199055-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151042948-C-G

33199150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151043011-C-T

33199191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151043052-T-C

33199388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151043231-A-G

33199720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151043579-A-G

33199731-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151043590-A-T

33199757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151043617-G-T

33199758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151043618-G-T

33199938-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151043787-G-C

33200117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151043963-G-A

33200457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151044458-G-A

33200457-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151044458-G-C

33200632-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151044627-T-G

http://identifiers.org/hco/13/GRCh38#33200645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#151044640-C-A

33200662-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151044647-C-G

33200662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151044647-C-T

33200701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151044684-A-G

33200719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151044702-C-T

33201129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151044737-T-C

33201208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151044827-C-T

http://identifiers.org/hco/13/GRCh38#33201343-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#151044940-A-C

33201343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151044940-A-G

33202765-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151047053-C-G

33202979-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 151047286-C-G

33203055-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 151047315-A-T

33203068-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 151047328-G-C

33203327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151047627-T-C

33203817-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151048080-C-G

33203888-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151048142-T-A

33204332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151049383-T-C

33204504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151049552-A-G

33204678-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151049721-C-G

http://identifiers.org/hco/13/GRCh38#33205397-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#151050370-A-C

33205691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151050691-T-C

33205707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151050710-T-C

33205732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151050736-T-C

http://identifiers.org/hco/13/GRCh38#33205746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#151050750-C-A

33205746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151050750-C-T

33205763-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151050767-G-C

33205763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151050767-G-T

33205859-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 151050861-A-T

http://identifiers.org/hco/13/GRCh38#33205862-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#151050864-A-C

33205869-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 151050871-T-A

http://identifiers.org/hco/13/GRCh38#33205951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#151050953-C-A

33206214-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151051230-G-C

33206225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151051241-C-T

33206476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151051494-G-A

33206518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151051532-A-G

33207015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151052413-T-C

33207095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151052490-G-A

33207275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151053003-A-G

33207275-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151053003-A-T

33207426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151053132-G-A

33207458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151053164-T-C

33207833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151053488-G-A

33207836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151053491-G-A

33210537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151054585-C-T

33210580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151054628-T-C

33210953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151056367-C-T

33211032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151056427-T-C

33211086-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151056480-T-G

33211231-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151056613-T-A

http://identifiers.org/hco/13/GRCh38#33211314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#151056646-C-A

33211340-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151056671-G-T

http://identifiers.org/hco/13/GRCh38#33211364-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#151056698-A-C

33211413-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151056730-T-A

33211413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151056730-T-C

33211938-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151056855-C-G

33212012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151056974-A-G

33212071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151057030-G-A

33212324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151057254-T-C

33212486-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151057364-T-A

33212541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151057397-G-T

33212567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151057422-C-T

33212647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151057505-T-C

33213455-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151058621-A-T

33213496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151058664-C-T

33213514-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151058682-G-C

33213514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151058682-G-T

33213554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151058700-G-A

33213614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151058759-A-G

33213755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151058892-G-T

33213896-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 151059036-T-A

33213967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 151059091-G-A

33214057-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151059164-G-C

33214097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151059217-G-A

33214133-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151059244-T-G

33214745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151059785-G-A

33214832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151059852-C-T

33214836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151059856-G-A

33215101-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151060107-A-T

33215126-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151060132-G-C

33215126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151060132-G-T

33222839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151061097-T-C

33222867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151061186-C-T

33223116-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151061466-T-G

33223332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151061676-A-G

33223833-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151061811-T-G

33224185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151062154-A-G

http://identifiers.org/hco/13/GRCh38#33228147-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#151064693-A-C

http://identifiers.org/hco/13/GRCh38#33228454-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#151064996-A-C

33228454-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151064996-A-T

33228455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151064997-G-T

33228504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151065057-T-C

33228601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151065759-A-G

http://identifiers.org/hco/13/GRCh38#33228803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#151065956-C-A

33228803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151065956-C-T

33228809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151065962-T-C

33228832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151065985-T-C

33228852-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151066005-G-C

33228866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151066019-G-A

33228967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151066118-A-G

33228967-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151066118-A-T

33229533-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151066641-C-G

33229644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151066687-T-C

33230021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151067059-G-A

33230138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151067159-C-T

33230195-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151067199-G-C

33230563-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151067536-C-G

33230850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151067804-C-T

33231004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151067970-G-A

33231026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151067992-T-C

http://identifiers.org/hco/13/GRCh38#33232552-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#151069218-A-C

33232552-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151069218-A-T

33234245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151069503-T-C

33234270-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151069529-C-G

33234317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151069575-C-T

33234389-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151069653-T-A

33234485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151069751-C-T

33234579-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151069839-T-G

33234854-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151070057-T-A

33235522-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151071356-G-C

33235639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151071458-C-T

33235757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151071557-G-A

33235793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151071593-G-A

33235818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151071618-C-T

33235898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151071677-C-T

33236286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 151071875-G-A

33236518-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151072064-A-T

33236568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151072120-C-T

33236644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151072188-T-C

33236649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151072193-G-A

33236649-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151072193-G-C

33245169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151072759-A-G

33245194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151072784-T-C

33245406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151073028-C-T

33245628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151073249-A-G

33245639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151073261-G-T

33245708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151073331-T-C

33245726-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151073349-T-A

33245764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151073387-T-C

33246008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151073535-C-T

33246297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151073822-C-T

33246313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151073838-G-A

33246314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151073839-G-A

33250313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151075363-A-G

33250461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151075521-A-G

33250462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151075522-G-A

33250572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151075633-T-C

33250662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151076183-T-C

33250697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151076218-C-T

33251053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 151076717-A-G

33251076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151076735-A-G

33251095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151076753-A-G

33251095-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151076753-A-T

33251139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 151076797-T-C

33251199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151076854-T-C

33251349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 151077203-G-T

33251365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 151077219-A-G

33251366-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 151077220-T-A

33251366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 151077220-T-C

33251369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 151077223-C-T

33251709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 151077541-G-A

33251820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151077641-C-T

33251947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151077805-T-C

33252471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151078488-C-T

33252476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151078493-G-A

33252525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151078507-C-T

33252579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151078948-G-T

33252671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151079040-G-A

33252671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151079040-G-T

33252786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151079155-T-C

33252786-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151079155-T-G

33252837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151079214-C-T

33252838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151079215-G-A

33253016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151079382-C-T

33253408-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151079770-A-T

33253412-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151079774-A-T

33253517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151079884-G-A

33253567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151079936-C-T

33253599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151079965-C-T

33253609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151079973-G-A

33253609-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151079973-G-C

33253611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151079975-T-C

33253679-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151080016-T-G

http://identifiers.org/hco/13/GRCh38#33253803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#151080149-C-A

33253803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151080149-C-T

33253908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151080241-A-G

33253930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151080263-G-A

33254006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151080350-C-T

33256591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151082408-G-A

33256719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151082517-G-A

33257195-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151082974-G-C

33257444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151083213-C-T

33257534-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151083357-C-G

33257534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151083357-C-T

33257602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151083407-T-C

33257821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151083620-A-G

33257881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151083679-A-G

33257944-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151083744-T-A

33257944-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151083744-T-G

33258343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151084093-T-C

33258372-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151084120-A-T

33258373-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151084121-C-G

33258972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151084503-T-C

33259095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151084623-A-G

33259451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151084991-A-G

33259451-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151084991-A-T

33261517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151087718-C-T

33261891-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151088089-T-A

33261891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151088089-T-C

33261893-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151088091-C-G

33261893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151088091-C-T

33262276-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 151088441-G-C

http://identifiers.org/hco/13/GRCh38#33262606-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#151088719-A-C

33262993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151089258-C-T

33263043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151089297-T-C

33263116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151089367-C-T

33263176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151089423-G-A

33263351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151089582-C-T

33263378-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151089613-C-G

33264125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151091439-C-T

33264854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 151092047-C-T

33264887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151092077-A-G

http://identifiers.org/hco/13/GRCh38#33264954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#151092143-C-A

33264954-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151092143-C-G

33265048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151092239-G-A

33265048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151092239-G-T

33266298-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151093530-T-A

33266298-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151093530-T-G

33266508-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151093712-C-G

33266725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151093925-C-T

http://identifiers.org/hco/13/GRCh38#33266726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#151093926-C-A

33267003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151094772-A-G

33267320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151095109-A-G

33267497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151095267-G-A

33267545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151095292-G-A

33267769-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151095472-T-G

33267832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151095537-C-T

33268296-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151095948-A-T

33268569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151096170-A-G

33268787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151096355-C-T

http://identifiers.org/hco/13/GRCh38#33269416-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#151096949-A-C

33269567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151097074-A-G

33269876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151097349-A-G

33270573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151097701-A-G

33270627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151097754-G-A

33271290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151098354-T-C

33271481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 151098524-G-T

33271491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 151098534-G-T

33271494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 151098537-G-A

33271494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 151098537-G-T

33271630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151098651-T-C

33271854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151098853-T-C

33271919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151098919-G-A

33272003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151099004-C-T

33272137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151099133-C-T

33272140-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151099136-A-T

http://identifiers.org/hco/13/GRCh38#33272489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#151099286-C-A

33272489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151099286-C-T

33272627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 151099417-G-A

33272630-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 151099420-T-A

33272630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 151099420-T-C

33272647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 151099436-A-G

33272719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 151099503-A-G

33273334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151100366-T-C

33273845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151102802-G-A

http://identifiers.org/hco/13/GRCh38#33273870-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#151102826-A-C

33274266-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151103531-T-A

http://identifiers.org/hco/13/GRCh38#33274292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#151103555-C-A

33274292-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151103555-C-G

33274292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151103555-C-T

33274317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151103580-T-C

33274359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151103618-G-A

33274359-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151103618-G-C

33274837-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151104036-T-A

33274855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151104056-T-C

33275025-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151104213-T-G

http://identifiers.org/hco/13/GRCh38#33275156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#151104318-C-A

33275993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 151104863-G-A

33276004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 151104872-G-A

33276004-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 151104872-G-C

33276004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 151104872-G-T

33276013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 151104881-T-C

33276190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 151105037-G-A

33276190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 151105037-G-T

33276345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151105189-T-C

33276345-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151105189-T-G

33276658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151105661-G-A

33276684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 151105687-G-A

33276694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 151105697-G-A

33276745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 151105708-T-C

33276792-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151105746-T-A

33276798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151105752-C-T

33276801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151105755-G-T

http://identifiers.org/hco/13/GRCh38#33276866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#151105821-C-A

33276866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151105821-C-T

33276899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151105851-G-T

33276934-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151105884-A-T

33276969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151105919-T-C

http://identifiers.org/hco/13/GRCh38#33277038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#151105994-C-A

33277038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151105994-C-T

33277113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151106113-T-C

33277162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151106146-G-T

33277235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151106218-G-A

33277235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 151106218-G-T

33277328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 151106317-T-C

33277346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 151106335-T-C

http://identifiers.org/hco/13/GRCh38#33277385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#151106373-C-A

http://identifiers.org/hco/13/GRCh38#33277445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#151106454-C-A

33277445-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 151106454-C-G

33277462-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 151106485-A-T

33277501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 151106518-C-T

http://identifiers.org/hco/13/GRCh38#33277540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#151106544-C-A

33277540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 151106544-C-T

33277590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 151106590-T-C

33277599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 151106599-G-T

33277627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 151106626-G-T

33277769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 151106771-T-C

http://identifiers.org/hco/13/GRCh38#33277813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#151106811-C-A

33277887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 151106909-A-G

33278013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 151107187-T-C

33278249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 151107428-G-A

http://identifiers.org/hco/13/GRCh38#33278274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#151107452-C-A

33278336-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 151107513-T-G

http://identifiers.org/hco/13/GRCh38#33278435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#151107594-C-A

33278435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 151107594-C-T

http://identifiers.org/hco/13/GRCh38#33278488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#151107648-C-A

33280005-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 151108762-T-A

33280005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 151108762-T-C

33280036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 151108795-T-C

http://identifiers.org/hco/13/GRCh38#33280057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#151108815-C-A

33280057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 151108815-C-T

http://identifiers.org/hco/13/GRCh38#33280109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#151108867-C-A

http://identifiers.org/hco/13/GRCh38#33280187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#151108931-C-A

33280187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 151108931-C-T

33280203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 151108955-T-C

33280203-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 151108955-T-G

http://identifiers.org/hco/13/GRCh38#33280507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#151109233-C-A

33280507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 151109233-C-T

33280610-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 151109317-A-T

33280914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 151109593-T-C

33280951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 151109629-A-G

33281003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 151109672-A-G

33281117-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 151109777-T-A

33281117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 151109777-T-C

33281344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 151110022-A-G

33281348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 151110026-T-C

33281363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 151110041-G-T

33281395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 151110075-G-T

33281542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 151110142-A-G

33281577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 151110177-T-C

33281577-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 151110177-T-G