76435239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 5 prime UTR variant
orthologous variants: 92830746-T-C

76435315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 5 prime UTR variant
orthologous variants: 92830802-C-T

76435501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 5 prime UTR variant
orthologous variants: 92831015-C-T

76435520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 5 prime UTR variant
orthologous variants: 92831034-T-C

76435545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 5 prime UTR variant
orthologous variants: 92831059-G-A

76435765-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 5 prime UTR variant
orthologous variants: 92831301-T-G

76436195-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 92831665-A-T

http://identifiers.org/hco/4/GRCh38#76436294-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92831781-A-C

76436302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92831789-G-T

http://identifiers.org/hco/4/GRCh38#76436305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92831828-C-A

76436305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92831828-C-T

76436589-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92832110-C-G

76436589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92832110-C-T

76436666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92832187-G-A

76436797-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92832449-A-T

76436798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92832450-G-T

76437064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92832907-C-T

76437313-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92833203-A-T

76437473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92833356-G-A

76437514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92833399-C-T

76437549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92833434-C-T

http://identifiers.org/hco/4/GRCh38#76438351-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92834546-A-C

76438369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92834558-G-A

76438474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92834657-A-G

http://identifiers.org/hco/4/GRCh38#76439035-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92835261-A-C

76439035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92835261-A-G

76439129-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92835355-T-A

76439222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92835511-T-C

76439230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92835519-T-C

76439543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92836094-G-A

76440048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92836609-T-C

76440084-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92836645-A-T

76440128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92836684-C-T

76440199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92836749-G-A

76440272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92836806-G-A

76441440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92837954-G-T

http://identifiers.org/hco/4/GRCh38#76441490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92838011-C-A

76442224-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92838582-C-G

76442240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92838599-A-G

76442282-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92838646-A-T

76442783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92838869-T-C

76442848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92838919-G-A

76442848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92838919-G-T

76443097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92839738-G-A

76443113-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92839754-A-T

76443323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92839962-T-C

76443426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92840065-A-G

76443536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92840170-C-T

76443554-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92840183-A-T

76445175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92840823-C-T

76445204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92840907-C-T

76445219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92840922-T-C

76445352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92841026-G-A

76445352-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92841026-G-C

76445355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92841029-A-G

76445508-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92841192-A-T

76445540-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92841221-T-G

76447384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92842191-G-T

76447803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92842648-A-G

http://identifiers.org/hco/4/GRCh38#76448371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92843134-C-A

http://identifiers.org/hco/4/GRCh38#76448485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92843258-C-A

76448614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92843370-G-A

76448775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92844357-A-G

76448853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92844437-T-C

76449584-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92844567-C-G

76451635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92847763-T-C

76459296-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92846559-G-C

76459304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92846550-A-G

76459452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92846401-A-G

76459488-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92846358-G-C

76459548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92846304-A-G

http://identifiers.org/hco/4/GRCh38#76465822-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92849191-A-C

76466203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92849468-A-G

76466587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92849817-G-A

76466620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92849853-G-T

76466893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92850135-A-G

76467258-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92850411-G-C

76467400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92850530-G-A

76467766-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92850784-A-T

76470299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92851256-A-G

76470431-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92851396-C-G

76470601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92851532-G-A

76470697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92851661-T-C

76476057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92854227-A-G

76476395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92854547-C-T

76476407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92854559-C-T

76476409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92854560-C-T

76477332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92855102-T-C

76477350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92855120-T-C

76477411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92855200-C-T

76477454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92855264-T-C

76477465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92855383-C-T

76477531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92855448-T-C

76477601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92855538-A-G

76477648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92855586-C-T

76484587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92855827-A-G

76484901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92856157-G-A

76485038-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92856255-C-G

http://identifiers.org/hco/4/GRCh38#76485050-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92856268-A-C

76485209-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92856400-C-G

http://identifiers.org/hco/4/GRCh38#76485455-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92856738-A-C

76485574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92856876-T-C

76485635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92856937-T-C

76485660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92856962-G-A

76485687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92857003-G-A

http://identifiers.org/hco/4/GRCh38#76485776-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92857093-A-C

76485776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92857093-A-G

76485797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92857098-A-G

76485843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92857139-A-G

76485843-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92857139-A-T

76486469-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92858381-A-T

76486717-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92858818-G-C

76486857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92858961-G-T

http://identifiers.org/hco/4/GRCh38#76486923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92859026-C-A

76486945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92859048-T-C

http://identifiers.org/hco/4/GRCh38#76487016-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92859121-A-C

76487016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92859121-A-G

http://identifiers.org/hco/4/GRCh38#76487023-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92859128-A-C

76487023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92859128-A-G

http://identifiers.org/hco/4/GRCh38#76487066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92859164-C-A

http://identifiers.org/hco/4/GRCh38#76487320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92859399-C-A

76487608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92859623-C-T

76487683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92859698-G-T

76488009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92860020-A-G

http://identifiers.org/hco/4/GRCh38#76488063-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92860074-A-C

76488063-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92860074-A-T

76488301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92860302-G-A

76488477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92860468-C-T

http://identifiers.org/hco/4/GRCh38#76488564-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92860537-A-C

76488579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92860552-T-C

76488927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92860897-C-T

76489033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92860975-T-C

76491969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92863069-C-T

76492017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92863135-G-A

76492052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92863167-C-T

76492140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92863256-A-G

76492149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92863265-G-T

76492411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92863484-A-G

76492415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92863488-A-G

76492470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92863542-G-A

http://identifiers.org/hco/4/GRCh38#76492620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92864485-C-A

76492663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92864536-G-A

76492691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92864564-T-C

76494226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92865770-A-G

76494545-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92866125-T-G

76494547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92866127-A-G

76495107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92866777-C-T

76495270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92866966-T-C

76495303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92867002-C-T

76495384-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92867196-T-G

76495389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92867201-G-A

76495629-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92867422-T-G

76495753-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92867529-G-C

76496229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92868401-G-A

76496367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92868477-G-A

76496712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92868754-A-G

76496712-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92868754-A-T

http://identifiers.org/hco/4/GRCh38#76496783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92868822-C-A

76496783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92868822-C-T

76496923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92869605-T-C

76497018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92869699-A-G

76498022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92870636-T-C

76498181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92870792-G-T

76498598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92871207-C-T

76498906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92871505-G-A

76498906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92871505-G-T

76498919-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92871518-G-C

76499129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92871760-T-C

76499173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92871805-C-T

76499331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92871955-A-G

76499331-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92871955-A-T

http://identifiers.org/hco/4/GRCh38#76499355-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92871979-A-C

76499399-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92872017-G-C

76499487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92872088-A-G

http://identifiers.org/hco/4/GRCh38#76499541-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92872130-A-C

76499541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92872130-A-G

76499557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92872141-T-C

76499572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92872156-G-A

76499572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92872156-G-T

http://identifiers.org/hco/4/GRCh38#76499580-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92872164-A-C

76503129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92872673-G-A

76503354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92872899-G-A

76503354-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92872899-G-C

76503354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92872899-G-T

76503416-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92872951-T-A

76503431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92872966-T-C

76503746-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92873175-A-T

76505120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92874013-A-G

76511676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92876646-T-C

76511676-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92876646-T-G

76511703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92876667-A-G

76511719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92876683-G-T

76511745-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92876709-T-A

76512418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92877254-T-C

76512476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92877283-G-T

76512623-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92877394-C-G

76512647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92877418-T-C

76512649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92877420-G-A

76513204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92878058-G-T

76513209-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92878062-C-G

76513908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92878763-T-C

76514074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92878916-T-C

http://identifiers.org/hco/4/GRCh38#76514744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92880232-C-A

76514744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92880232-C-T

http://identifiers.org/hco/4/GRCh38#76515507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92880796-C-A

76515596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92880876-C-T

76515896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92881687-A-G

76515901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92881692-G-A

76516020-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92881811-A-T

76516068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92881860-T-C

76516178-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92881968-A-T

76516268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92882053-A-G

76516378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92882161-C-T

76516432-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92882214-T-A

76516493-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92882279-C-G

76516563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92882345-G-T

76516668-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92882463-C-G

76517103-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92883128-G-C

76517216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92883209-G-A

76517620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92883776-G-T

76517967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92884028-G-A

76518223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92884440-A-G

76518351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92884573-A-G

76518359-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92884581-T-G

http://identifiers.org/hco/4/GRCh38#76518399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92884618-C-A

76518453-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92884673-T-G

76518972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92885020-T-C

76519072-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92885108-C-G

76519201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92885220-C-T

76519276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92885294-G-T

76519692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92885660-A-G

76519703-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92885671-T-G

76519941-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92885849-C-G

76519970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92885877-A-G

76520345-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92886238-A-T

76520543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92886461-A-G

76520619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92886536-A-G

76520754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92887069-T-C

76524113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92890153-C-T

76524210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92890242-G-A

76524246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92890276-G-A

76524261-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92890293-T-G

http://identifiers.org/hco/4/GRCh38#76524404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92890434-C-A

76524404-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92890434-C-G

76524444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92890474-A-G

76524517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92890553-G-T

76524528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92890585-A-G

76524552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92890610-C-T

76524676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92890723-G-A

76524769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92890788-G-A

76524776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92890795-A-G

76524786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92890809-G-A

76524788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92890811-C-T

76524795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92890818-T-C

76524897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92890913-C-T

76524911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92890926-A-G

76525832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92892884-T-C

76525861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92892913-C-T

76525903-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92892953-T-G

http://identifiers.org/hco/4/GRCh38#76526583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92893672-C-A

76527104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92894168-A-G

http://identifiers.org/hco/4/GRCh38#76527115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92894181-C-A

76527803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92895169-C-T

http://identifiers.org/hco/4/GRCh38#76527848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92895213-C-A

76527902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92895266-C-T

76527939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92895308-G-A

76527985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92895358-C-T

76528002-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92895374-A-T

http://identifiers.org/hco/4/GRCh38#76528199-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92895575-A-C

76528927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92895760-C-T

76528960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92895784-G-T

http://identifiers.org/hco/4/GRCh38#76529004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92895827-C-A

76529004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92895827-C-T

76529043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92895867-T-C

76529046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92895878-C-T

76529073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92895904-C-T

76529129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92895956-G-A

76529142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92895970-T-C

76529254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92896072-T-C

76529277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92896093-A-G

76529299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92896113-G-A

76530225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92896876-A-G

76530406-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92897018-T-A

76530674-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92897262-G-C

76530720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92897301-A-G

76530740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92897319-C-T

76530756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92897336-A-G

76530756-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92897336-A-T

76530805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92897379-G-A

76530923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92897469-A-G

76530928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92897475-A-G

76530940-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92897487-A-T

76531085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92897605-A-G

76531287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92898564-A-G

76531503-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92898775-G-C

http://identifiers.org/hco/4/GRCh38#76531607-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92898861-A-C

76531612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92898866-G-A

76532396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92899191-T-C

76532417-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92899216-A-T

76535621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92900002-A-G

76535697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92900079-C-T

76535701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92900083-C-T

76535704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92900086-T-C

76535720-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92900102-C-G

76535720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92900102-C-T

http://identifiers.org/hco/4/GRCh38#76535727-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92900109-A-C

76535756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92900139-T-C

http://identifiers.org/hco/4/GRCh38#76535762-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92900145-A-C

76535825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92900204-C-T

76536103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92900393-A-G

76536146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92900434-A-G

76536219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92900503-G-A

http://identifiers.org/hco/4/GRCh38#76536383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92900666-C-A

http://identifiers.org/hco/4/GRCh38#76536414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92900709-C-A

76536475-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92900775-G-C

76536475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92900775-G-T

76538350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92909766-T-C

http://identifiers.org/hco/4/GRCh38#76538706-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92910130-A-C

76538946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92910358-T-C

http://identifiers.org/hco/4/GRCh38#76539339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92911036-C-A

76539339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92911036-C-T

http://identifiers.org/hco/4/GRCh38#76539458-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92911275-A-C

76540172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92911670-G-A

http://identifiers.org/hco/4/GRCh38#76540358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92911846-C-A

76540358-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92911846-C-G

76541218-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92912779-G-C

76543945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92914240-T-C

76544898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92915246-G-A

76545066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92915388-A-G

76545066-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92915388-A-T

76545404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92915702-C-T

76545502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92915804-C-T

76545651-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92915956-A-T

http://identifiers.org/hco/4/GRCh38#76545652-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92915957-A-C

76545652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92915957-A-G

76545781-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92916075-A-T

76546112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92917692-C-T

76546180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92917755-A-G

76546190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92917765-C-T

76546205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92917780-T-C

76546335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92917894-G-T

76546390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92917948-C-T

76546413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92917969-G-A

http://identifiers.org/hco/4/GRCh38#76546574-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92918123-A-C

76546583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92918132-T-C

76546622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92918172-A-G

76546636-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92918180-G-C

76546684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92918582-A-G

76546728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92918627-A-G

76546993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92918885-C-T

76547008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92918900-G-A

76547025-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92918914-C-G

76547030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92918919-C-T

76547041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92918930-G-A

76547061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92918950-A-G

76547061-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92918950-A-T

76547065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92918954-G-A

76547104-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92918993-T-G

76547165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92919054-C-T

76547374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92919270-A-G

76547377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92919279-T-C

76547416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92919322-G-T

76547421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92919331-G-A

76547504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92919415-G-A

76547581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92919484-C-T

76548810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92920819-T-C

76548814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92920823-C-T

76548818-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92920827-C-G

76548818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92920827-C-T

76548819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92920828-G-A

76548873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92920875-C-T

76548927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92920937-G-A

http://identifiers.org/hco/4/GRCh38#76548951-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92920961-A-C

76549083-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92921087-T-A

76549088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92921092-G-A

76549088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92921092-G-T

76549491-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92921338-C-G

76549668-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92921512-T-A

76549719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92921562-A-G

76549850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92921683-A-G

76550336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92922177-A-G

http://identifiers.org/hco/4/GRCh38#76550477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92922313-C-A

76550482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92922318-T-C

76551428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92924616-T-C

76551639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92924779-T-C

76551650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92924783-G-A

76551650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92924783-G-T

76551679-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92924814-G-C

76551679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92924814-G-T

76551825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92924957-C-T

76555279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92928314-G-A

http://identifiers.org/hco/4/GRCh38#76555389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92928400-C-A

76555389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92928400-C-T

76555390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92928401-G-A

76555390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92928401-G-T

76555576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92928582-A-G

http://identifiers.org/hco/4/GRCh38#76555635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92928638-C-A

76555635-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 92928638-C-G

76557380-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92929535-T-G

76557734-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92930091-T-G

76558051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92930591-T-C

76558103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92930634-T-C

76558129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92930655-G-A

76558304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92930815-C-T

76558418-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92930948-C-G

http://identifiers.org/hco/4/GRCh38#76558511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92931022-C-A

76558525-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92931035-T-G

76558675-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92931183-C-G

http://identifiers.org/hco/4/GRCh38#76558695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92931203-C-A

76558978-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92931378-A-T

76559015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92931413-A-G

76559030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92931428-T-C

76559263-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 92931647-G-T

http://identifiers.org/hco/4/GRCh38#76559284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#92931669-C-A

76559334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 92931714-G-A

76559334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 92931714-G-T

76559597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92931995-T-C

76559851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92932209-A-G

76559926-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92932278-G-C

76559926-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92932278-G-T

76559966-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92932306-G-C

76562094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92933741-T-C

76562095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92933742-G-A

76562289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92933912-C-T

76562294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92933917-G-A

76562878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92935038-T-C

76562964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92935107-G-T

76563342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92935497-G-T

76563442-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92935687-G-C

76563473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92935717-G-A

http://identifiers.org/hco/4/GRCh38#76563521-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92935751-A-C

76563532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92935762-A-G

76563577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92935820-G-A

76564254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92936851-G-T

76564328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92936925-G-A

76564332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92936929-A-G

76564340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92936937-G-A

76564540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92937136-C-T

76564617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92937213-G-A

76564638-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92937233-C-G

76564740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92937330-G-A

76566956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92939435-A-G

76566973-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92939452-T-A

76567144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92939614-T-C

76567733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92939767-G-T

http://identifiers.org/hco/4/GRCh38#76567841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92939880-C-A

76567841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92939880-C-T

76567842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92939881-G-A

76568032-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92940038-C-G

76568163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92940218-G-A

76568186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92940294-C-T

76570083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92944274-G-A

76570281-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92944451-G-T

76570450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92944621-C-T

76570529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92944696-A-G

76570905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92945321-G-A

76570912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92945328-A-G

http://identifiers.org/hco/4/GRCh38#76571153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92945784-C-A

76571155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92945786-G-A

76571159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92945790-T-C

76571694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92946304-G-A

76572072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92946635-A-G

76572258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92947239-G-A

76572279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92947260-A-G

76572330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92947318-G-A

76572444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92947441-G-A

76572686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92947671-G-A

76572731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92947717-T-C

76580113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92950877-T-C

76580185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92950946-T-C

76580261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92951010-A-G

76580376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92951088-A-G

76580429-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92951112-G-C

76580429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92951112-G-T

76581116-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92951634-C-G

76581132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92951652-T-C

76581218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92951731-C-T

76581441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92951948-T-C

76581497-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92951996-C-G

76581497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92951996-C-T

76581563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92952041-G-A

76581605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92952083-G-A

76581924-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92952412-C-G

76582001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92953151-A-G

http://identifiers.org/hco/4/GRCh38#76582203-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92953368-A-C

76582388-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92953620-T-A

76582446-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92953676-T-A

76583246-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92954572-T-G

76583375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92954703-G-A

76583608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92954869-T-C

http://identifiers.org/hco/4/GRCh38#76583694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92954955-C-A

76583694-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92954955-C-G

76583778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92955026-T-C

76583799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92955039-A-G

76584572-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92955321-A-T

76584617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92955364-G-A

76584710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92955463-A-G

http://identifiers.org/hco/4/GRCh38#76584881-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92955940-A-C

76585046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92956111-C-T

76585148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92956206-A-G

http://identifiers.org/hco/4/GRCh38#76585220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92956259-C-A

76585237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92956276-C-T

76585254-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92956293-C-G

76585729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92956718-G-A

76585972-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92956952-G-C

76586036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92957017-A-G

http://identifiers.org/hco/4/GRCh38#76586047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#92957028-C-A

76586047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92957028-C-T

76586142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 92957113-A-G

76586142-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 92957113-A-T

76586164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 92957135-G-T

76586208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92957180-T-C

76586215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 92957186-T-C

76586266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 92957235-G-T

76586274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 92957243-C-T

76586307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 92957276-G-A

76586322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92957284-T-C

http://identifiers.org/hco/4/GRCh38#76586371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#92957327-C-A

76586371-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 92957327-C-G

76586412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92957363-G-T

76586715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92957613-G-A

http://identifiers.org/hco/4/GRCh38#76586827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92957722-C-A

76587049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92957913-G-T

http://identifiers.org/hco/4/GRCh38#76587097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92957956-C-A

76587270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92958054-G-T

76587476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92958222-C-T

76587575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92958347-G-A

76587897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92958648-T-C

76588058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92958797-C-T

76588109-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92958842-A-T

76588121-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92958854-A-T

http://identifiers.org/hco/4/GRCh38#76588321-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92959028-A-C

76588349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92959055-G-A

76588349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92959055-G-T

76588622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92959282-C-T

76588624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92959284-T-C

76588729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92959374-C-T

http://identifiers.org/hco/4/GRCh38#76588861-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92959506-A-C

76589068-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92959685-C-G

76589068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92959685-C-T

76589621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92959916-G-T

76589888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92960196-A-G

76589901-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92960209-T-A

76590256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92960801-T-C

76590281-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92960826-C-G

76590281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92960826-C-T

76590335-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92960888-C-G

76590335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92960888-C-T

76592682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92963023-A-G

76592891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92963224-C-T

http://identifiers.org/hco/4/GRCh38#76592927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92963248-C-A

76593081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92963406-C-T

76593086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92963411-A-G

76593086-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92963411-A-T

76593330-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92963561-T-G

76593803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92963947-G-A

76594209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92964343-C-T

76594301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92964559-A-G

76594354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92964613-A-G

76594956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92965215-A-G

76595061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92967010-G-A

76595394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92967443-G-A

76595404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92967453-G-A

76595485-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92967483-C-G

76595511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92967509-G-A

http://identifiers.org/hco/4/GRCh38#76595645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92967746-C-A

76595645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92967746-C-T

76595944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92968024-G-T

76595981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92968062-G-T

76596842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92968495-G-A

76596854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92968507-C-T

76596977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92968624-A-G

http://identifiers.org/hco/4/GRCh38#76597015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92968661-C-A

76597015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92968661-C-T

76597046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92968693-A-G

http://identifiers.org/hco/4/GRCh38#76597280-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92968916-A-C

76597280-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92968916-A-T

76597460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92969057-T-C

76597503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92969096-A-G

76597793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92969350-G-A

76597966-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92969517-G-C

76598431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92970672-A-G

76598431-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92970672-A-T

76598512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92970753-A-G

76598591-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92970835-T-A

76598778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92970996-A-G

76598793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92971011-C-T

76598794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92971012-A-G

76598818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92971037-A-G

76598965-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92971293-G-T

76598966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92971294-G-A

76598966-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92971294-G-C

76598966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92971294-G-T

76599191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92971495-C-T

76599233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92971535-G-A

76599292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92971583-C-T

76599300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92971591-T-C

76600546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92972605-A-G

76600664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92972706-G-A

http://identifiers.org/hco/4/GRCh38#76601941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92974298-C-A

76602014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92974355-T-C

76602403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92974784-A-G

http://identifiers.org/hco/4/GRCh38#76605434-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92977351-A-C

76605440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92977357-G-T

76605466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92977383-C-T

76605644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92977534-C-T

76605804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92977883-C-T

http://identifiers.org/hco/4/GRCh38#76605908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92977990-C-A

http://identifiers.org/hco/4/GRCh38#76606768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92978277-C-A

76606768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92978277-C-T

76606786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92978295-G-T

76606804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92978313-A-G

76607009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92978519-G-A

76607117-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92978682-T-A

76607117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92978682-T-C

76607311-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92978857-C-G

76607321-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92978867-C-G

76607321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92978867-C-T

76607337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92978883-A-G

76607459-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92979004-G-C

76607629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92979184-G-A

76607695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92979231-G-A

76607695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92979231-G-T

76607702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92979241-A-G

76608089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92979616-C-T

76608093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92979619-C-T

http://identifiers.org/hco/4/GRCh38#76608305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92979852-C-A

76608371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92979925-C-T

76608842-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92980194-C-G

76608842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92980194-C-T

76608880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92980231-G-T

76608970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92980408-A-G

76608992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92980431-A-G

76609038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92980479-A-G

76609880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92982977-A-G

76609991-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92983080-T-G

76610133-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92983199-T-A

76610172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92983237-A-G

76610221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92983284-A-G

76610285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92983359-G-A

76610368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92983456-G-A

76610419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92983504-T-C

76610463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92983614-G-A

76610747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92983859-G-A

76610833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92983949-C-T

76610942-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92984055-A-T

76611826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92985055-T-C

http://identifiers.org/hco/4/GRCh38#76611841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92985070-C-A

76611841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92985070-C-T

76611980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92985157-G-A

76612061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92985236-A-G

76613114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92986133-G-A

76613285-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92986311-A-T

76613286-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92986312-T-G

76613411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92986440-T-C

76613554-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92986671-T-G

76613681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92986763-G-T

76613739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92986820-G-T

76613745-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92986826-T-A

http://identifiers.org/hco/4/GRCh38#76615371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92987316-C-A

76615387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92987332-T-C

76615429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92987365-C-T

76615430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92987366-G-A

76615536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92987465-C-T

76619324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92988733-G-T

76619476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92988893-A-G

http://identifiers.org/hco/4/GRCh38#76619760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92989134-C-A

76619760-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92989134-C-G

76622442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92989644-A-G

http://identifiers.org/hco/4/GRCh38#76622566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92989770-C-A

76622566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92989770-C-T

76622574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92989778-A-G

76622585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92989790-T-C

76622632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92990060-G-A

76622678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92990173-C-T

76622843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92990390-G-A

76622939-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92990506-T-G

76622940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92990515-G-T

76623056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92990617-A-G

76623232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92990789-G-A

76623242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 92990799-T-C

76623262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92990819-G-A

76623514-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92991038-C-G

76623796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92991333-G-A

76623926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92991422-C-T

76623948-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92991451-A-T

76624015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92991533-C-T

76624095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92991608-C-T

76624530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92992049-C-T

76624691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92992217-G-A

76624874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92992563-T-C

76624874-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92992563-T-G

76625143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92992791-G-T

http://identifiers.org/hco/4/GRCh38#76625171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92992820-C-A

76625265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92992915-C-T

76625361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92993016-G-A

76625545-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92993241-T-G

http://identifiers.org/hco/4/GRCh38#76625600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92993297-C-A

76625669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92993342-G-A

76626072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92994291-G-T

76626733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92995285-G-A

76626836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92995393-A-G

76627142-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92995839-C-G

76627142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92995839-C-T

76627353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92996027-C-T

76627454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92996125-C-T

76627553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92996219-C-T

76630912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92996325-A-G

76631054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92996481-A-G

76631056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92996483-G-A

76631615-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92996656-T-G

76632075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92997110-T-C

76632124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92997212-G-A

http://identifiers.org/hco/4/GRCh38#76632157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92997245-C-A

76632157-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92997245-C-G

76632184-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92997272-T-G

76632216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92997304-G-A

76632301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92997383-G-A

76632312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92997398-G-A

76632501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92997576-A-G

76632538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92997612-G-A

76633037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92997974-G-A

76634329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92998832-G-T

76634906-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92999382-T-A

76635298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92999718-A-G

76635540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92999922-T-C

76635561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92999943-C-T

76635627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93000018-G-A

76635627-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93000018-G-C

76635778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93000174-A-G

76635888-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93000240-G-C

76635997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93000347-G-A

76636298-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93001130-A-T

76636299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93001131-C-T

76636319-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93001140-T-G

76636349-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93001171-T-G

76636413-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93001250-G-C

76636489-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93001329-T-G

http://identifiers.org/hco/4/GRCh38#76637150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93001367-C-A

76637541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93002434-T-C

76637568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93002459-G-T

76637615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93002507-A-G

http://identifiers.org/hco/4/GRCh38#76637631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93002523-C-A

76637696-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93002801-T-A

http://identifiers.org/hco/4/GRCh38#76637746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93002841-C-A

76637746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93002841-C-T

76637866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93002942-A-G

76638037-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93003116-A-T

http://identifiers.org/hco/4/GRCh38#76638038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93003117-C-A

http://identifiers.org/hco/4/GRCh38#76638041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93003120-C-A

http://identifiers.org/hco/4/GRCh38#76639481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#93004297-C-A

76639481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93004297-C-T

76639485-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93004301-G-C

76639485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93004301-G-T

76639533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93004342-T-C

http://identifiers.org/hco/4/GRCh38#76639536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#93004345-C-A

76639676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93004482-T-C

76639761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93004545-T-C

76639793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93004577-A-G

76639851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93004628-A-G

76639929-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93004708-T-G

76639949-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93004724-C-G

76639949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93004724-C-T

76640123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93004882-A-G

76640134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93004893-A-G

76640275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93005056-C-T

76640315-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93005095-T-A

76640452-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93005235-A-T

76640488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93005268-T-C

76640552-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93005327-C-G

76640752-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93005526-A-T

76640783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93005554-C-T

76640808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93005579-C-T

76640923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93005677-G-A

76641505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93006233-C-T

76641558-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93006285-T-A

76641558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93006285-T-C

76641566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93006293-G-T

http://identifiers.org/hco/4/GRCh38#76641573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93006300-C-A

76641573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93006300-C-T

76641608-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93006334-G-C

76641696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93006422-C-T

76641926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93006648-C-T

76642112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93006844-G-A

76642134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93006864-A-G

76642439-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93007771-G-T

76642487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93007804-A-G

76642589-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93007898-A-T

76642590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93007899-A-G

76642761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93008101-G-T

76643186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93008223-C-T

76643223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93008230-A-G

http://identifiers.org/hco/4/GRCh38#76643432-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93008439-A-C

76643500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93008506-A-G

76643527-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93008533-C-G

http://identifiers.org/hco/4/GRCh38#76643797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93009082-C-A

76644739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93009305-T-C

http://identifiers.org/hco/4/GRCh38#76644740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93009306-C-A

76644791-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93009356-C-G

76644820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 93009385-C-T

76644855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93009425-C-T

76644875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93009445-G-A

http://identifiers.org/hco/4/GRCh38#76645099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93009669-C-A

http://identifiers.org/hco/4/GRCh38#76645215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93009783-C-A

76645215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93009783-C-T

76645225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93009793-T-C

http://identifiers.org/hco/4/GRCh38#76645295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
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#93009871-C-A

76645297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 93009873-A-G

76645313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93009890-T-C

http://identifiers.org/hco/4/GRCh38#76645369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93009955-C-A

76645369-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93009955-C-G

76645369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93009955-C-T

http://identifiers.org/hco/4/GRCh38#76645405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93009984-C-A

76645433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93010004-T-C

76645461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93010029-G-A

76645461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93010029-G-T

76645498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93010067-A-G

http://identifiers.org/hco/4/GRCh38#76645729-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93010275-C-A

76646190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93010874-G-A

http://identifiers.org/hco/4/GRCh38#76646201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93010885-C-A

76646201-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93010885-C-G

76646233-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93010927-T-A

http://identifiers.org/hco/4/GRCh38#76646421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93011199-C-A

76646421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93011199-C-T

http://identifiers.org/hco/4/GRCh38#76646631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93011375-C-A

76646648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93011392-G-A

76648524-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93012032-C-G

76648584-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93012089-C-G

http://identifiers.org/hco/4/GRCh38#76648692-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93012200-A-C

76648692-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93012200-A-T

76648827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93012315-G-A

76648876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93012624-G-A

76648876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93012624-G-T

76648888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93012636-A-G

76649055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93012810-G-A

76649055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93012810-G-T

76649147-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93012900-C-G

76649312-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93013063-T-G

76649483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93013211-G-A

76649485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93013213-T-C

http://identifiers.org/hco/4/GRCh38#76649867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93013554-C-A

76650000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93013658-C-T

76650001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93013659-G-A

76650001-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93013659-G-T

76650014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93013671-T-C

76651516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93014557-A-G

76651550-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93014591-G-C

76651550-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93014591-G-T

76651885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93014895-C-T

76651920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93014930-G-A

76652170-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93015155-A-T

76652388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93015364-G-A

76652389-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93015365-C-G

76652551-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93015527-G-C

76653101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93016175-G-A

76654755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93017371-G-A

76654755-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93017371-G-C

76655283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93017882-G-T

http://identifiers.org/hco/4/GRCh38#76655376-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93017978-A-C

76655376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93017978-A-G

76655480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93018074-G-T

76655516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93018108-A-G

76655523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93018115-G-A

76655532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93018124-G-A

76655652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93018230-G-A

76655652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93018230-G-T

76657546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93020141-T-C

76657547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93020142-T-C

76657825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93020379-C-T

76657904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93020457-G-T

76658249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93020736-C-T

76658976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93021674-C-T

76659389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93022025-C-T

76663415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93025305-A-G

76663439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93025329-A-G

76663441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93025330-C-T

http://identifiers.org/hco/4/GRCh38#76663855-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93026457-A-C

76664495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93027597-G-T

76664585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93027681-G-A

76664789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93027933-T-C

76665301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93028316-G-A

76665781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93028775-G-A

76665874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93028853-C-T

76665952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93028929-C-T

76666058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93029033-A-G

76666125-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93029096-G-C

76666171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93029142-C-T

76666172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93029143-G-A

76674951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93034099-T-C

76675081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93034228-G-A

76675256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93034425-C-T

76675559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93035040-A-G

76677649-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93035479-C-G

76677649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93035479-C-T

76677912-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93035727-C-G

76677914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93035729-T-C

76677953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93035769-G-A

76678260-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93036044-A-T

76678272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93036056-T-C

76678377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93036139-T-C

76678395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93036157-C-T

76678448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93036203-T-C

76678598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93036360-G-T

76678843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93036419-G-T

76678950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93036470-C-T

76679301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93036786-C-T

76679386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93036841-C-T

76679468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93036957-T-C

http://identifiers.org/hco/4/GRCh38#76679561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93037283-C-A

76679756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93037441-A-G

http://identifiers.org/hco/4/GRCh38#76679776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93037474-C-A

http://identifiers.org/hco/4/GRCh38#76679839-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93037542-A-C

76679897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93037588-T-C

76679904-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93037595-T-A

76679918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93037609-C-T

http://identifiers.org/hco/4/GRCh38#76680134-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93037794-A-C

76680134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93037794-A-G

76680134-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93037794-A-T

76680142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93037802-C-T

76680505-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93037858-C-G

76680505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93037858-C-T

http://identifiers.org/hco/4/GRCh38#76680680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93038045-C-A

76680680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93038045-C-T

76680904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93038254-T-C

http://identifiers.org/hco/4/GRCh38#76680905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93038255-C-A

76680953-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93038304-T-G

76681081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93038425-T-C

76681469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93038763-T-C

http://identifiers.org/hco/4/GRCh38#76681635-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93038938-A-C

76681635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93038938-A-G

76681653-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93038964-G-T

76681728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93039040-C-T

76681849-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93039156-T-G

76682542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93040460-T-C

76682642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93040575-G-A

76682647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93040580-A-G

76682993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93040877-G-A

76683117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93040948-T-C

76684355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93041424-C-T

76684374-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93041440-C-G

76684423-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93041495-T-A

76684427-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93041499-T-G

http://identifiers.org/hco/4/GRCh38#76684491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93041585-C-A

76684973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93042077-G-T

76684986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93042091-T-C

76684994-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93042096-G-C

76685066-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93042172-C-G

76685193-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93042291-C-G

76685529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93042380-C-T

76686510-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93042877-G-C

76686640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93043001-T-C

76686715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93043272-C-T

76686836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93043394-C-T

76687086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93043571-G-A

76687614-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93044118-T-G

76687647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93044154-C-T

76687867-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93044402-T-G

http://identifiers.org/hco/4/GRCh38#76688227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93044774-C-A

76688227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93044774-C-T

76688341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93044869-T-C

76688341-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93044869-T-G

http://identifiers.org/hco/4/GRCh38#76688348-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93044876-A-C

76688348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93044876-A-G

76688363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93044892-C-T

76688562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93045056-G-A

http://identifiers.org/hco/4/GRCh38#76688592-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93045088-A-C

76688592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93045088-A-G

76688629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93045126-C-T

76688857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93045335-G-T

76689024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93045513-A-G

76689024-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93045513-A-T

76689042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93045531-T-C

76689178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93045640-G-A

76689210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93045657-G-A

76689296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93045739-C-T

76689462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93045897-T-C

76689502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93045913-C-T

76689512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93045923-C-T

76689526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93045934-C-T

76689553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93045964-G-A

76689611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93046020-C-T

76689692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93046069-G-A

76689692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93046069-G-T

76689728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93046102-G-A

76689728-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93046102-G-C

76689728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93046102-G-T

http://identifiers.org/hco/4/GRCh38#76689786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93046169-C-A

76689786-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93046169-C-G

76689786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93046169-C-T

76689790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93046173-G-A

76689790-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93046173-G-C

76689790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93046173-G-T

http://identifiers.org/hco/4/GRCh38#76689792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93046175-C-A

76689792-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93046175-C-G

76689807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93046193-T-C

76689807-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93046193-T-G

76689811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93046197-G-A

76689815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93046201-A-G

76689817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93046203-G-A

76689817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93046203-G-T

76689824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93046210-A-G

76690036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93046420-C-T

76690703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93047007-C-T

http://identifiers.org/hco/4/GRCh38#76690967-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93047259-A-C

76690967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93047259-A-G

76691462-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93047725-G-C

76691467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93047730-G-A

76691467-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93047730-G-C

76691827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93048401-C-T

76691862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93048445-A-G

76692170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93048733-A-G

76692204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93048749-G-A

76692204-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93048749-G-C

76692220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93048770-A-G

76692245-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93048795-G-C

76692490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93049031-T-C

76692853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93049500-A-G

http://identifiers.org/hco/4/GRCh38#76693334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93049898-C-A

76693334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93049898-C-T

http://identifiers.org/hco/4/GRCh38#76693645-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93050423-A-C

76693674-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93050456-T-G

http://identifiers.org/hco/4/GRCh38#76694017-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93050787-C-A

76694039-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93050809-C-G

76694267-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93051158-G-C

76694273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93051164-A-G

76694538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93051415-A-G

76694717-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93051569-A-T

76694763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93051616-A-G

76694858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93051717-A-G

76694966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93051830-C-T

76694997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93051856-A-G

76696182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93053388-T-C

76696294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93053482-C-T

76696357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93053543-A-G

76696521-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93053706-A-T

76696768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93053943-A-G

76697454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93054464-G-A

76697509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93054518-G-T

76697613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93054621-G-A

76697914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93054994-T-C

76698090-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93055376-T-A

76698550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93056009-G-A

76698682-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93056126-A-T

76698771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93056206-A-G

76698950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93056354-T-C

76699011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93056389-A-G

76699090-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93056470-T-G

76699206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93056579-A-G

76699246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93056616-G-A

76699280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93056636-G-A

http://identifiers.org/hco/4/GRCh38#76699298-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93056662-A-C

76699298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93056662-A-G

76699319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93056674-A-G

76699328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93056683-G-A

76699428-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93056766-T-G

76700159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93057091-A-G

76700160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93057092-T-C

76700220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93057146-C-T

76700342-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93057250-C-G

76700384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93057287-T-C

76700576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93057437-C-T

76700620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93057484-T-C

76700663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93057532-G-A

76700790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93057654-T-C

76701357-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93058122-G-T

76701580-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93058345-A-T

76701742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93058491-C-T

http://identifiers.org/hco/4/GRCh38#76701930-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93058640-A-C

http://identifiers.org/hco/4/GRCh38#76702428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93058884-C-A

76702428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93058884-C-T

76702596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93059053-A-G

76702700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93059156-G-A

76702713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93059169-T-C

76702910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93059579-A-G

76702910-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93059579-A-T

76703477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93060119-T-C

76703625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93060623-A-G

76703789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93060787-A-G

76703864-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93061389-T-A

76704031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93061513-G-A

76704103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93061553-C-T

76704216-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93061633-A-T

76704540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93061934-G-T

76705015-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93062268-A-T

76705053-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93062299-G-C

76705180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93062424-A-G

76705609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93062501-A-G

76705617-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93062505-T-A

76705694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93062601-C-T

76707489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93063455-C-T

76707609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93063566-A-G

76708209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93063798-T-C

http://identifiers.org/hco/4/GRCh38#76708227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93063816-C-A

76708348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93063941-G-A

76708353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93063946-G-A

76708353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93063946-G-T

http://identifiers.org/hco/4/GRCh38#76708407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93063991-C-A

76708407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93063991-C-T

76708415-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93063999-T-G

http://identifiers.org/hco/4/GRCh38#76709122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93066103-C-A

76709122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93066103-C-T

76709198-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93066176-C-G

76709208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93066186-G-A

76709641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93066917-G-T

76709795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93067082-G-A

76709795-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93067082-G-C

76709795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93067082-G-T

http://identifiers.org/hco/4/GRCh38#76709957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93067344-C-A

76709957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93067344-C-T

76709969-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93067350-T-G

76710042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93067396-T-C

76710096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93067442-T-C

76710100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93067446-T-C

76710119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93067466-C-T

76710120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93067467-A-G

76710423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93067740-A-G

76711600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93068230-G-A

76711684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93068336-A-G

76714218-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93070875-C-G

76714254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93070913-C-T

76714488-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93071633-G-C

76714869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93072013-A-G

76714875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93072019-G-A

76714875-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93072019-G-C

76714900-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93072044-A-T

http://identifiers.org/hco/4/GRCh38#76714983-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93072111-A-C

76715186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93072282-T-C

76715389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93072510-G-A

76715480-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93072615-C-G

76715737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93072823-A-G

http://identifiers.org/hco/4/GRCh38#76716213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93073155-C-A

76716250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93073197-G-A

76716320-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93073258-A-T

76716322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93073260-C-T

76716348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93073286-G-A

76716348-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93073286-G-C

76716348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93073286-G-T

76716374-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93073306-G-C

76716465-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93073383-C-G

76716465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93073383-C-T

76716590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93073703-T-C

76716722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93073839-A-G

76716736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93073853-C-T

76717263-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93075210-G-T

76717324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93075267-T-C

http://identifiers.org/hco/4/GRCh38#76718201-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93075995-A-C

76718292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93076074-A-G

76718432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93076222-T-C

http://identifiers.org/hco/4/GRCh38#76718790-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93076537-A-C

76718831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93076569-T-C

76718859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93076597-C-T

http://identifiers.org/hco/4/GRCh38#76718879-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93076620-A-C

76720051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93077152-G-A

76720051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93077152-G-T

76720059-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93077162-C-G

76720059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93077162-C-T

76722962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93077933-G-A

http://identifiers.org/hco/4/GRCh38#76723133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93078601-C-A

76723169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93078642-T-C

76728771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93080317-C-T

76730058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93080976-C-T

76730203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93081090-G-A

76730268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93081156-C-T

76730432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93081335-T-C

76730765-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93081573-T-G

76730813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93081622-G-A

76730972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93081781-T-C

http://identifiers.org/hco/4/GRCh38#76731226-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93081975-A-C

76731247-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93081996-T-G

76731292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93082039-G-A

76732114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93082595-A-G

76732317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93082780-C-T

76732412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93082856-C-T

76732498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93082923-T-C

76732522-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93082948-T-A

76732601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93083023-G-A

76732601-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93083023-G-C

76732603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93083025-G-A

76732693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93083092-A-G

76732741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93083115-G-A

76732743-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93083117-C-G

76732743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93083117-C-T

76732783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93083157-C-T

http://identifiers.org/hco/4/GRCh38#76732860-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93083230-A-C

76733021-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93083353-T-G

76733033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93083365-G-A

76733156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93083489-A-G

76733410-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93083711-G-C

76733474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93083772-T-C

76733474-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93083772-T-G

76733735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93084002-C-T

76733746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93084014-C-T

76733784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93084048-G-A

76733796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93084060-G-A

76734298-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93084518-T-A

76734341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93084546-T-C

76734456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93084658-T-C

76734516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93084732-T-C

76734602-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93084827-C-G

76734826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93085100-G-A

76734906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93085172-T-C

76734974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93085244-C-T

76735000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93085269-A-G

76735014-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93085279-C-G

76735098-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93085362-T-A

76735301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93085535-A-G

76735344-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93085579-C-G

76735504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93085734-T-C

76736443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93086230-C-T

http://identifiers.org/hco/4/GRCh38#76736589-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93086366-A-C

76736589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93086366-A-G

76738184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93087253-C-T

76738284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93087352-G-A

76738305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93087373-C-T

http://identifiers.org/hco/4/GRCh38#76738306-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#93087374-A-C

76738306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93087374-A-G

http://identifiers.org/hco/4/GRCh38#76738369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93087446-C-A

76738369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93087446-C-T

http://identifiers.org/hco/4/GRCh38#76738591-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93087681-A-C

http://identifiers.org/hco/4/GRCh38#76738709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93087783-C-A

http://identifiers.org/hco/4/GRCh38#76738791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93087866-C-A

76738863-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93087938-G-C

76739160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93088238-G-A

76739331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93088409-A-G

76739365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93088443-C-T

http://identifiers.org/hco/4/GRCh38#76739541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93088619-C-A

76739541-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93088619-C-G

76739655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93088733-A-G

76739748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93088826-G-A

76739748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93088826-G-T

76739787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93088865-G-A

http://identifiers.org/hco/4/GRCh38#76739898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93088970-C-A

76739898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93088970-C-T

76739946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93089018-C-T

76739950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93089022-A-G

76739962-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93089037-T-A

76739979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93089054-C-T

http://identifiers.org/hco/4/GRCh38#76740008-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93089083-A-C

76740048-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93089123-C-G

76740048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93089123-C-T

76740126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93089201-G-A

http://identifiers.org/hco/4/GRCh38#76740238-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93089310-C-A

76740238-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93089310-C-G

76740368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93089425-C-T

http://identifiers.org/hco/4/GRCh38#76740415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93089472-C-A

76740415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93089472-C-T

76740426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93089483-G-A

76740426-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93089483-G-C

76740426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93089483-G-T

76740435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93089492-C-T

76740451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93089508-G-A

76740474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93089531-G-A

76740474-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93089531-G-C

76740474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93089531-G-T

76740495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93089543-C-T

76740584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93089635-G-A

76740585-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93089636-T-A

http://identifiers.org/hco/4/GRCh38#76740609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93089660-C-A

76740609-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93089660-C-G

76740609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93089660-C-T

http://identifiers.org/hco/4/GRCh38#76740618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93089669-C-A

76740618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93089669-C-T

76740622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93089673-A-G

76740677-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93089731-C-G

76740677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93089731-C-T

76740746-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93089800-C-G

76740752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93089814-G-A

76740771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93089838-G-A

76740778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93089850-G-A

76740789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93089861-G-A

76740789-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93089861-G-T

http://identifiers.org/hco/4/GRCh38#76740798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93089870-C-A

76740798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93089870-C-T

http://identifiers.org/hco/4/GRCh38#76740900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93089975-C-A

76740930-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93090005-C-G

76740930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93090005-C-T

76740948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93090023-G-A

76740948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93090023-G-T

76740966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93090041-A-G

76740966-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93090041-A-T

76741017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93090092-G-A

76741017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93090092-G-T

http://identifiers.org/hco/4/GRCh38#76741100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93090178-C-A

76741100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93090178-C-T

76741143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93090221-T-C

76741245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93090302-G-A

76741285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93090342-G-A

76741285-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93090342-G-C

76741299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93090356-G-A

76741299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93090356-G-T

76741313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93090373-T-C

http://identifiers.org/hco/4/GRCh38#76741389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93090449-C-A

76741389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93090449-C-T

http://identifiers.org/hco/4/GRCh38#76741401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93090461-C-A

76741401-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93090461-C-G

76741401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93090461-C-T

76741413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93090473-G-A

76741413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93090473-G-T

http://identifiers.org/hco/4/GRCh38#76741427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93090487-C-A

76741427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93090487-C-T

http://identifiers.org/hco/4/GRCh38#76741455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93090515-C-A

76741455-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93090515-C-G

76741455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93090515-C-T

76741468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93090528-A-G

http://identifiers.org/hco/4/GRCh38#76741491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93090545-C-A

76741491-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93090545-C-G

76741491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93090545-C-T

76741518-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93090569-C-G

76741518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93090569-C-T

76741519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93090570-G-A

76741519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93090570-G-T

http://identifiers.org/hco/4/GRCh38#76741536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93090587-C-A

76741543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93090594-G-A

76741543-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93090594-G-C

76741543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93090594-G-T

76741551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93090602-G-A

76741551-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93090602-G-C

76741551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93090602-G-T

http://identifiers.org/hco/4/GRCh38#76741566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93090617-C-A

76741566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93090617-C-T

76741578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93090629-G-A

76741578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93090629-G-T

76741584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93090635-C-T

76741613-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93090664-T-A

76741613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93090664-T-C

76741614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93090665-G-A

76741614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93090665-G-T

76741633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93090684-A-G

76741653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93090698-T-C

76741677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93090722-A-G

76741757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93090820-G-A

76741757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93090820-G-T

http://identifiers.org/hco/4/GRCh38#76741791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93090854-C-A

76741815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93090884-C-T

http://identifiers.org/hco/4/GRCh38#76741839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93090911-C-A

76741839-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93090911-C-G

76741839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93090911-C-T

76741860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93090932-G-A

76741860-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93090932-G-C

76741860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93090932-G-T

76741885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93090957-G-A

76741885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93090957-G-T

76741967-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93091040-C-G

76741985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93091059-T-C

76742079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93091145-T-C

http://identifiers.org/hco/4/GRCh38#76742083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93091149-C-A

76742089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93091155-T-C

76742106-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93091180-T-A

76742106-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93091180-T-G

76742107-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93091181-T-A

76742107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93091181-T-C

76744317-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93092347-T-A

76744693-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93092749-T-A

76744892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93092871-C-T

76744940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93092907-G-A

76744940-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93092907-G-C

http://identifiers.org/hco/4/GRCh38#76745323-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93093293-A-C

76745449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93093356-G-A

76745486-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93093384-C-G

76745572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93093456-A-G

76745655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93093543-G-A

76747392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93094673-T-C

76747631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93094985-G-A

76747982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93095317-A-G

http://identifiers.org/hco/4/GRCh38#76747993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93095333-C-A

76748118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93095438-G-A

76748205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93095875-G-A

76749041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93096287-G-A

76749042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93096288-G-T

76753246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93097390-A-G

http://identifiers.org/hco/4/GRCh38#76753566-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93097689-A-C

76754037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93098183-G-T

76754047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93098193-C-T

76754151-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93098271-T-G

76754270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93098302-T-C

http://identifiers.org/hco/4/GRCh38#76754359-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93098391-C-A

76754359-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93098391-C-G

76754360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93098392-C-T

76754434-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93098466-T-G

76754435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93098467-G-A

76754463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93098492-G-A

76754470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93098499-A-G

76754618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 93098647-C-T

76754675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 93098677-C-T

76754721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 93098723-A-G

76754789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 93098791-G-A

76754800-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 93098802-G-C

http://identifiers.org/hco/4/GRCh38#76754839-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93098841-A-C

76754871-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 93098873-T-A

http://identifiers.org/hco/4/GRCh38#76755073-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93099054-A-C

76755073-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93099054-A-T

http://identifiers.org/hco/4/GRCh38#76755127-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93099111-A-C

76755159-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 93099146-T-A

76755159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 93099146-T-C

76755185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 93099172-C-T

http://identifiers.org/hco/4/GRCh38#76755243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93099234-C-A

76755258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93099242-G-A

http://identifiers.org/hco/4/GRCh38#76755264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93099248-C-A

76755264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93099248-C-T

http://identifiers.org/hco/4/GRCh38#76755271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93099255-C-A

76755271-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93099255-C-G

76755271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93099255-C-T

http://identifiers.org/hco/4/GRCh38#76755283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93099267-C-A

76755283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93099267-C-T

76755326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93099308-T-C

76755380-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93099352-T-G

76755647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93099629-G-A

http://identifiers.org/hco/4/GRCh38#76755688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93099670-C-A

76755688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93099670-C-T

76755691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93099673-C-T

76755730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93099702-G-T

76755731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93099703-G-A

http://identifiers.org/hco/4/GRCh38#76756300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93100279-C-A

76756300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93100279-C-T

76756301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93100280-A-G

76756328-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93100303-A-T

http://identifiers.org/hco/4/GRCh38#76756333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93100308-C-A

http://identifiers.org/hco/4/GRCh38#76756334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93100309-C-A

http://identifiers.org/hco/4/GRCh38#76756354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93100322-C-A

76756354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93100322-C-T

76756358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93100326-G-A

76756551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93100503-T-C

76756552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93100504-A-G

76756562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93100514-C-T

76756570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93100522-G-A

76756597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93100549-G-A

76756597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93100549-G-T

76756652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93100604-A-G

76756701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93100653-A-G

76756711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93100663-G-A

76756711-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93100663-G-C

76756809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93100761-C-T

76756812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93100764-G-A

76756845-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93100797-G-C

76756954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93100906-G-A

76756990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93100938-G-A

76756990-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93100938-G-C

76757041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93100979-G-A

76757041-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93100979-G-C

76757098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93101020-A-G

http://identifiers.org/hco/4/GRCh38#76757157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93101073-C-A

76757157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93101073-C-T

76757408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93101265-C-T

76757470-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93101325-C-G

76757470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93101325-C-T

76757598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93101445-C-T

76757884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93101776-G-A

76757941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93101833-G-A

76758088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93101975-G-A

76758165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93102048-T-C

76758227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93102107-C-T

76758241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93102121-G-A

http://identifiers.org/hco/4/GRCh38#76758309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93102226-C-A

76758790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93102632-A-G

76759341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93102984-G-T

76759509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93103106-T-C

76759512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93103109-G-A

76759680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93103255-T-C

76759764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93103326-G-A

76759764-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93103326-G-C

76759764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93103326-G-T

76759793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93103359-G-A

76760181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93103608-C-T

76760229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93103656-G-A

76760504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93103888-T-C

76760569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93103946-G-A

76766375-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93107675-T-A

76766378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93107678-T-C

76766578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93107866-G-A

76768875-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93109223-G-C

76770490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93109821-G-A

76770490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93109821-G-T

http://identifiers.org/hco/4/GRCh38#76770499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93109831-C-A

76770499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93109831-C-T

76770519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93109848-T-C

76770537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93109866-A-G

http://identifiers.org/hco/4/GRCh38#76770576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93109902-C-A

76770880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93110204-T-C

76770886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93110210-T-C

76774926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93111244-T-C

76777886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93111461-C-T

76778707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93112133-G-A

76778707-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93112133-G-C

76778767-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93112174-C-G

76778850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93112256-T-C

http://identifiers.org/hco/4/GRCh38#76778859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93112265-C-A

76778880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93112286-G-A

76778931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93112337-G-A

76779096-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93112502-C-G

76779096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93112502-C-T

76779126-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93112532-T-G

76779129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93112535-G-A

76779141-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 93112547-C-G

76779141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93112547-C-T

76779146-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 93112552-G-C

76779146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 93112552-G-T

http://identifiers.org/hco/4/GRCh38#76779178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93112584-C-A

http://identifiers.org/hco/4/GRCh38#76779198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93112604-C-A

76779198-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93112604-C-G

http://identifiers.org/hco/4/GRCh38#76779257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93112659-C-A

76779257-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93112659-C-G

76779258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93112660-T-C

76779259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93112661-G-A

76779259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93112661-G-T

76779278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93112678-T-C

76779295-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93112693-T-A

76779349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93112735-G-T

76779373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93112759-G-T

76779415-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93112767-A-T

76779449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93112799-G-A

76779449-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93112799-G-T

76779452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93112802-G-A

76779452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93112802-G-T

76779483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93112830-C-T

76780029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93113537-G-T

76780084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93113579-A-G

http://identifiers.org/hco/4/GRCh38#76780094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93113589-C-A

76780094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93113589-C-T

76780250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93113703-G-T

76780324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93113774-G-T

76780325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93113775-G-T

76780333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93113787-G-A

76780333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93113787-G-T

76780392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93113844-G-T

76780469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93113877-T-C

76780713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93113912-A-G

76780736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93113929-T-C

76780745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93113938-G-T

76780751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93113944-A-G

76780811-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93113992-A-T

76780832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93114016-G-T

http://identifiers.org/hco/4/GRCh38#76780853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93114030-C-A

76780873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93114051-G-A

76780873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93114051-G-T

76780907-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93114068-T-A

76780907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93114068-T-C

http://identifiers.org/hco/4/GRCh38#76780950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93114097-C-A

76780950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93114097-C-T

http://identifiers.org/hco/4/GRCh38#76781427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93114661-C-A

76781485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93114712-T-C

76781529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93114750-T-C

76781536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93114757-G-A

76781616-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93114839-T-G

76781814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93115030-A-G

76781948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93115138-C-T

76781950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93115140-C-T

76781981-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93115159-G-C

76781981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93115159-G-T

76782031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93115205-G-A

76782031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93115205-G-T

76782093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93115245-G-T

76782180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93115325-G-A

http://identifiers.org/hco/4/GRCh38#76782252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93115366-C-A

76782270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93115397-G-T

http://identifiers.org/hco/4/GRCh38#76782284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93115411-C-A

76782284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93115411-C-T

http://identifiers.org/hco/4/GRCh38#76782396-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93115466-A-C

76782682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93116048-C-T

76782709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93116075-A-G

76782770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93116135-G-A

76782796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93116149-A-G

76782961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93116879-G-A

76782961-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93116879-G-C

76782968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93116886-A-G

76782986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93116904-G-A

76782988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93116906-T-C

http://identifiers.org/hco/4/GRCh38#76782992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93116910-C-A

76782992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93116910-C-T

76783004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93116923-T-C

http://identifiers.org/hco/4/GRCh38#76783069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93117054-C-A

76783094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93117182-A-G

76783118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30422
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93117206-C-T