http://identifiers.org/hco/12/GRCh38#113816950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120338871-C-A

113817055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120338763-G-A

113817055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120338763-G-T

http://identifiers.org/hco/12/GRCh38#113817060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120338758-C-A

113817156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120338667-A-G

113817190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120338631-T-C

113823184-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120336082-T-G

http://identifiers.org/hco/12/GRCh38#113823187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120336079-C-A

113823187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120336079-C-T

113824449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120335316-G-A

http://identifiers.org/hco/12/GRCh38#113825073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120334803-C-A

113826356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120334008-C-T

http://identifiers.org/hco/12/GRCh38#113826602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120333713-C-A

113826975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120333400-G-A

113827288-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120333100-T-G

113827683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120332767-G-A

113831861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120330863-G-A

113832609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120330593-C-T

http://identifiers.org/hco/12/GRCh38#113832626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120330576-C-A

113833063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120330137-C-T

113833138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120330064-G-A

113833139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120330063-C-T

113833361-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120329875-T-G

113833386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120329847-C-T

113833406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120329822-G-A

113833588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120329630-T-C

113833691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120329524-G-A

113833691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120329524-G-T

113834795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120329241-C-T

113834878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120329162-A-G

113835199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120328873-C-T

113835873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120328265-C-T

113836021-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120328128-T-G

113836031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120328118-C-T

113836245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120327895-G-A

113836311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120327783-T-C

113839074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120326850-G-A

http://identifiers.org/hco/12/GRCh38#113839311-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120326632-A-C

113842145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120326376-C-T

113842320-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120326198-C-G

113842363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120326163-G-A

113842595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120325922-G-A

http://identifiers.org/hco/12/GRCh38#113842605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120325912-C-A

113842605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120325912-C-T

113842617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120325900-C-T

113844814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120324255-G-A

113844833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120324236-G-T

113844835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120324234-G-A

113844835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120324234-G-T

http://identifiers.org/hco/12/GRCh38#113844850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120324219-C-A

113844850-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120324219-C-G

113844850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120324219-C-T

113844913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120324188-T-C

113844916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120324185-T-C

113845400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120323836-C-T

113845432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120323808-C-T

http://identifiers.org/hco/12/GRCh38#113845467-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120323772-A-C

113845520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120323747-T-C

113845523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120323744-T-C

113847178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120322547-C-T

http://identifiers.org/hco/12/GRCh38#113847469-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120322229-C-A

113847500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120322180-G-T

113847590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120322113-C-T

113847708-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120322000-G-C

113847724-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120321984-C-G

113847729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120321979-C-T

113847786-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120321944-C-G

113847898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120321864-T-C

113848128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120321647-T-C

113848471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120321322-G-A

113848695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120321125-G-A

113848695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120321125-G-T

113848884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120321024-T-C

113848884-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120321024-T-G

113849155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120320821-G-A

113849793-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120320338-T-A

113849793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120320338-T-C

113849871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120320279-C-T

113849892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120320257-G-A

113849993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120320184-G-A

113849993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120320184-G-T

113850185-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120320046-T-G

113852368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120318175-C-T

113852473-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120318073-C-G

113852473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120318073-C-T

113852780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120317777-C-T

113852840-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120317676-C-G

113852840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120317676-C-T

113852884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120317631-T-C

113852913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120317608-G-A

113852914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120317607-A-G

113852929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120317592-C-T

http://identifiers.org/hco/12/GRCh38#113852958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120317564-C-A

113852958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120317564-C-T

113853189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120317402-C-T

http://identifiers.org/hco/12/GRCh38#113853549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120317074-C-A

113853618-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120316996-G-C

113853618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120316996-G-T

113853710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120316902-T-C

113853834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120316714-C-T

113853835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120316713-T-C

113853977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120316596-G-A

113854370-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120316380-C-G

113854370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120316380-C-T

113854499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120316281-T-C

113854499-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120316281-T-G

113854504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120316277-A-G

113854797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120316156-A-G

113854935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120316038-C-T

113855229-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120315802-C-G

113855229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120315802-C-T

113855470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120315620-G-A

113855485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120315609-G-A

113855486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120315608-G-T

113855626-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120315492-G-C

113855626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120315492-G-T

113855859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120315347-A-G

113855997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120315215-G-A

113855997-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120315215-G-C

113855997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120315215-G-T

113856122-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120315072-C-G

113856131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120315065-G-A

113858861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120313957-T-C

113858941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120313878-G-A

113858941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120313878-G-T

http://identifiers.org/hco/12/GRCh38#113859027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120313796-C-A

113859027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120313796-C-T

http://identifiers.org/hco/12/GRCh38#113859041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120313755-C-A

113859041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120313755-C-T

113859532-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120313292-C-G

113859532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120313292-C-T

113860208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120312682-C-T

113860355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120312528-C-T

113860436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120312451-G-A

http://identifiers.org/hco/12/GRCh38#113860774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120312163-C-A

113860774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120312163-C-T

113860783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120312154-G-A

113860813-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120312132-C-G

113860813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120312132-C-T

113860838-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120312107-A-T

113860854-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120312091-T-A

113861062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120311938-G-A

113861343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120311715-G-T

113861375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120311712-C-T

113861519-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120311666-A-T

113861809-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120311412-T-A

113861823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120311398-T-C

http://identifiers.org/hco/12/GRCh38#113861828-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120311393-A-C

113861939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120311315-C-T

113862275-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120310990-C-G

113863811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120309815-C-T

113863836-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120309783-T-A

113864424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120309396-C-T

113864425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120309395-T-C

http://identifiers.org/hco/12/GRCh38#113865317-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120308867-A-C

113865403-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120308813-A-T

113865503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120308725-T-C

113865617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120308633-T-C

113865681-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120308592-A-T

113866232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120308173-A-G

113869671-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120305804-A-T

113869699-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120305776-G-T

113874154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120303633-T-C

113874548-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120303394-C-G

113874724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120303236-G-T

113874887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120302995-C-T

113875455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120302408-G-A

113875481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120302386-G-A

113875780-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120302187-C-G

113875780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120302187-C-T

113875801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120302166-T-C

113876351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120301750-G-A

113876360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120301741-C-T

113876454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120301663-T-C

113878191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120300387-T-C

113880463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120299684-G-A

http://identifiers.org/hco/12/GRCh38#113880694-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120299490-A-C

113881460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120298746-C-T

113881484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120298721-G-T

http://identifiers.org/hco/12/GRCh38#113888928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120295211-C-A

113889141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120295017-T-C

113889324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120294896-G-A

113889396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120294827-T-C

113889528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120294709-C-T

113889754-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120294513-G-C

113889805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120294463-T-C

113889889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120294376-G-A

113889889-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120294376-G-C

113889889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120294376-G-T

113890389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120293895-A-G

http://identifiers.org/hco/12/GRCh38#113890392-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120293892-A-C

113890635-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120293662-T-G

113891384-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120293255-G-C

113891442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120293219-G-T

113891733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120293023-G-A

113891820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120292973-A-G

113892218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120292607-G-T

113897703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120290989-T-C

http://identifiers.org/hco/12/GRCh38#113897778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120290927-C-A

113898056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120290685-C-T

113899834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120290354-T-C

113899840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120290348-G-A

113900558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120289823-T-C

113908414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120287281-G-A

113908811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120286892-C-T

113908902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120286789-C-T

113912304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120284814-C-T

113912312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120284806-A-G

113912522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120284604-T-C

113913029-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120284104-C-G

113913031-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120284102-A-T

113913219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120283915-G-A

113913560-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120283595-G-C

113913633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120283525-G-T

http://identifiers.org/hco/12/GRCh38#113913875-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120283288-A-C

113914186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120282844-G-A

113914252-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120282770-A-T

http://identifiers.org/hco/12/GRCh38#113914294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120282714-C-A

113914698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120282400-G-A

http://identifiers.org/hco/12/GRCh38#113914780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120282322-C-A

113914876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120282249-G-A

113914876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120282249-G-T

http://identifiers.org/hco/12/GRCh38#113914889-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120282236-C-A

http://identifiers.org/hco/12/GRCh38#113914911-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120282219-A-C

113914962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 120282182-T-C

113915183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120281960-T-C

http://identifiers.org/hco/12/GRCh38#113915229-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120281922-A-C

113915229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120281922-A-G

113918258-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120281657-A-T

113918284-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120281621-T-A

113918284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120281621-T-C

http://identifiers.org/hco/12/GRCh38#113918560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120281371-C-A

113918560-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120281371-C-G

113918560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120281371-C-T

113918621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120281319-C-T

http://identifiers.org/hco/12/GRCh38#113918708-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120281248-A-C

113918948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120281021-T-C

113919653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120280586-C-T

113919996-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120280332-T-A

113919999-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120280328-T-A

113920006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120280321-T-C

113920205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120280150-C-T

113920811-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120279486-T-A

113920811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120279486-T-C

113920811-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120279486-T-G

113924490-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120278825-G-C

113924490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120278825-G-T

http://identifiers.org/hco/12/GRCh38#113924586-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120278750-A-C

113924655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120278685-C-T

113924714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120278643-T-C

113924714-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120278643-T-G

http://identifiers.org/hco/12/GRCh38#113924741-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120278616-C-A

113924741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120278616-C-T

113927144-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120278343-C-G

113927144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120278343-C-T

113927300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120278210-G-A

113927300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120278210-G-T

http://identifiers.org/hco/12/GRCh38#113927431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120277969-C-A

113927431-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120277969-C-G

113927431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120277969-C-T

http://identifiers.org/hco/12/GRCh38#113927437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120277963-C-A

113927437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120277963-C-T

http://identifiers.org/hco/12/GRCh38#113927552-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120277835-A-C

http://identifiers.org/hco/12/GRCh38#113927616-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120277787-A-C

113927621-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120277763-A-T

113930105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120276855-G-A

113930105-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120276855-G-C

http://identifiers.org/hco/12/GRCh38#113930351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120276661-C-A

113930574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120276460-C-T

113930670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120276394-G-A

113930670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120276394-G-T

113930824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120276310-T-C

113930859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120276280-G-A

113931919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120275331-C-T

113932068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120275197-G-A

113932095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120275176-G-A

113932443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120274880-A-G

113932804-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120274759-G-C

113932827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120274737-G-A

113932827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120274737-G-T

113932873-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120274704-T-G

113932925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120274654-C-T

113933338-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120274324-T-A

113933338-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120274324-T-G

113933372-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120274242-A-T

113933403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120274206-C-T

113933404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120274205-A-G

113933425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120274173-C-T

http://identifiers.org/hco/12/GRCh38#113933503-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#120274085-A-C

113936903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120272041-A-G

http://identifiers.org/hco/12/GRCh38#113936945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120272007-C-A

113936945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120272007-C-T

113936996-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120271955-T-A

113937009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 120271942-G-A

113937015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120271936-G-T

113937149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120271812-G-T

113940072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120270993-T-C

113940093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120270972-T-C

113940098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120270967-C-T

http://identifiers.org/hco/12/GRCh38#113940232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120270815-C-A

113940232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120270815-C-T

http://identifiers.org/hco/12/GRCh38#113940249-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120270796-A-C

113940249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120270796-A-G

http://identifiers.org/hco/12/GRCh38#113940259-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120270786-A-C

113940259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120270786-A-G

113940261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120270784-T-C

113940279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120270768-G-A

113940279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120270768-G-T

http://identifiers.org/hco/12/GRCh38#113940298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120270753-C-A

113940298-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120270753-C-G

113940359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120270690-G-A

113940462-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120270562-G-C

113940482-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120270542-G-C

113940673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120270388-G-A

113942294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120270324-T-C

113942294-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120270324-T-G

113942296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120270322-G-A

113942296-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120270322-G-C

113942296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120270322-G-T

113945969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120269176-G-A

113945969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120269176-G-T

113945972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120269173-G-A

113946226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120268995-A-G

113946321-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120268918-T-A

113946797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120266763-T-C

http://identifiers.org/hco/12/GRCh38#113946838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120266725-C-A

113947480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120266231-G-T

113947686-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120265994-T-G

113947706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120265974-T-C

113947722-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120265959-T-G

113947770-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120265899-C-G

113947770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120265899-C-T

113947789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120265880-T-C

113947789-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120265880-T-G

113947980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120265741-G-A

113948990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120265074-G-A

113948991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120265073-G-A

113948991-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120265073-G-C

113948991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120265073-G-T

113949045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120265020-A-G

http://identifiers.org/hco/12/GRCh38#113949055-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120265008-A-C

113949082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120264991-G-A

http://identifiers.org/hco/12/GRCh38#113949167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120264940-C-A

113949167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120264940-C-T

113949176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120264931-T-C

113949204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120264904-G-T

113949266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120264846-G-A

113949531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120264610-C-T

113949783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120264506-G-A

113949948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120264382-G-A

113949948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120264382-G-T

113950072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120264319-G-A

113950072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120264319-G-T

http://identifiers.org/hco/12/GRCh38#113950167-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120264230-A-C

http://identifiers.org/hco/12/GRCh38#113950168-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120264229-A-C

113950422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120264090-C-T

113950497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120264036-C-T

113950512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120264024-C-T

113950854-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120263763-C-G

113950946-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120263713-C-G

113950946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120263713-C-T

113951257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120263579-C-T

113951510-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120263379-G-C

113951596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120263320-T-C

113951683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120263244-G-A

113951683-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120263244-G-C

http://identifiers.org/hco/12/GRCh38#113951754-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120263188-A-C

http://identifiers.org/hco/12/GRCh38#113951796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120263142-C-A

113951836-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120263124-G-C

113951931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120263040-G-A

113952017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120262983-C-T

113952535-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120262812-C-G

http://identifiers.org/hco/12/GRCh38#113955007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120262360-C-A

113955007-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120262360-C-G

113955007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120262360-C-T

113955014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120262353-T-C

http://identifiers.org/hco/12/GRCh38#113955033-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120262334-C-A

113955033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120262334-C-T

http://identifiers.org/hco/12/GRCh38#113955233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#120262192-C-A

113955238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120262187-G-A

113955238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120262187-G-T

113955272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120262165-G-T

113955275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120262162-G-A

113955275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120262162-G-T

113955278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120262160-C-T

113955282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120262156-G-T

113955302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120262136-A-G

113955304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120262134-G-A

113955304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120262134-G-T

113955314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120262124-G-A

113955314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120262124-G-T

113955535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120261987-T-C

113955617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120261945-T-C

113955620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120261942-G-A

http://identifiers.org/hco/12/GRCh38#113957766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120261228-C-A

113957766-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120261228-C-G

113957766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120261228-C-T

113957808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120261186-T-C

http://identifiers.org/hco/12/GRCh38#113957837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120261175-C-A

113957887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120261122-C-T

113957896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120261113-G-A

113957896-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120261113-G-C

http://identifiers.org/hco/12/GRCh38#113957970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120261036-C-A

113957970-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120261036-C-G

113957970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120261036-C-T

113958040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120260966-G-A

113958221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120260842-C-T

113958228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120260835-G-A

113958288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120260770-A-G

113959225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 120258351-C-T

113959265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120258299-T-C

113959423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120258152-G-A

113959446-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120258132-G-T

113959450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120258128-G-A

113959450-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120258128-G-T

http://identifiers.org/hco/12/GRCh38#113959493-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120258107-A-C

113959493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120258107-A-G

113959493-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120258107-A-T

http://identifiers.org/hco/12/GRCh38#113959550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120258093-C-A

113959550-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120258093-C-G

113959554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120258089-G-A

113959554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120258089-G-T

113959734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120258058-T-C

113959734-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120258058-T-G

113959750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120258042-C-T

113959900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120257961-C-T

http://identifiers.org/hco/12/GRCh38#113960006-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120257866-A-C

113960006-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120257866-A-T

113960020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120257852-T-C

113960091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120257782-G-A

113960101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120257772-G-A

113960258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120257616-G-A

113960258-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120257616-G-C

113960258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120257616-G-T

113960293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120257578-T-C

113960300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120257571-A-G

113960840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120257304-A-G

113962218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120256919-T-C

http://identifiers.org/hco/12/GRCh38#113962230-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#120256907-A-C

113962275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 120256862-T-C

113962275-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 120256862-T-G

113962297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120256840-C-T

113962426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120256711-G-A

113962453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120256682-G-A

113962453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120256682-G-T

113962492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120256651-G-A

113962492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120256651-G-T

http://identifiers.org/hco/12/GRCh38#113962508-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#120256644-A-C

113962530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120256621-G-A

113962546-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120256604-T-G

113962678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120256473-T-C

113962792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120256366-T-C

113966149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120254753-G-A

113966149-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29098
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120254753-G-C