http://identifiers.org/hco/3/GRCh38#39052093-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#119724043-C-A

39052093-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 119724043-C-G

39052093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 119724043-C-T

39052123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119724074-G-A

39052123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119724074-G-T

39052135-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119724086-T-G

http://identifiers.org/hco/3/GRCh38#39052300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#119724229-C-A

39052300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119724229-C-T

39052384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119724313-G-A

39052384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119724313-G-T

39053964-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119726146-G-C

39054469-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119726580-G-C

39054606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119726704-T-C

39062889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119731240-C-T

39063058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 119731360-T-C

39063322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119731625-A-G

39064035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119732075-C-T

39064056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119732096-G-A

39064082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119732122-G-A

39064088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119732128-G-A

39064240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119732281-C-T

39064758-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119732451-T-A

39064773-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119732475-T-A

39064867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119732559-G-A

39065280-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119732933-A-T

39065353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119732994-G-T

39065517-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119733093-G-C

http://identifiers.org/hco/3/GRCh38#39065601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#119733158-C-A

39065888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 119733421-A-G

39065898-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119733431-T-G

39065921-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119733458-C-G

39065921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119733458-C-T

39065950-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119733492-T-A

39065950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119733492-T-C

39065953-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119733495-T-A

39066175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119733947-C-T

39066176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119733948-G-A

39066400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119734157-A-G

39066400-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119734157-A-T

39066503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119734243-T-C

39066552-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 119734273-A-T

39066717-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119734405-T-A

39066717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119734405-T-C

39066720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 119734408-A-G

39066769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 119734457-T-C

39066814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 119734502-A-G

39066814-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119734502-A-T

39067161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119734830-G-A

39067430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119735084-T-C

39067469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119735121-G-A

39067597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119735231-G-A

39067641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119735272-C-T

39067948-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119735528-T-A

39068116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119735627-A-G

39068182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119735689-G-A

39068516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119735927-T-C

39068665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119736090-T-C

39068735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119736158-A-G

39068867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 119736289-G-A

http://identifiers.org/hco/3/GRCh38#39069510-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#119736621-A-C

http://identifiers.org/hco/3/GRCh38#39069576-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#119736685-A-C

39069581-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119736690-T-G

39069735-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 119736844-T-G

http://identifiers.org/hco/3/GRCh38#39069807-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#119736894-C-A

39069807-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119736894-C-G

39071562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119737442-A-G

39071569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119737449-A-G

39071590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119737470-C-T

http://identifiers.org/hco/3/GRCh38#39073054-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#119737746-A-C

39074972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119738657-T-C

39074988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119738673-G-A

39074988-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119738673-G-T

http://identifiers.org/hco/3/GRCh38#39075392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#119738931-C-A

39076399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119739263-G-A

39076580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119739411-G-A

39076828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119739717-A-G

http://identifiers.org/hco/3/GRCh38#39077013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#119739947-C-A

39077072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119740027-T-C

39077079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119740034-T-C

39077272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119740226-T-C

39077920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119741220-A-G

39077920-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119741220-A-T

39077959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119741264-T-C

39077978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119741292-T-C

39077978-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119741292-T-G

39077995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119741307-G-A

39077995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119741307-G-T

http://identifiers.org/hco/3/GRCh38#39077999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#119741311-C-A

39078018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119741325-T-C

39078022-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119741332-G-C

39078184-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 119741480-T-A

39078203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 119741499-A-G

39078203-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 119741499-A-T

http://identifiers.org/hco/3/GRCh38#39078246-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#119741542-A-C

39078246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 119741542-A-G

http://identifiers.org/hco/3/GRCh38#39078361-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#119741652-A-C

39078361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119741652-A-G

39078361-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119741652-A-T

39078379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119741670-T-C

http://identifiers.org/hco/3/GRCh38#39079918-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#119742865-A-C

39079918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119742865-A-G

39079918-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119742865-A-T

39081767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119743248-G-T

http://identifiers.org/hco/3/GRCh38#39082077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#119743530-C-A

39082079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119743532-A-G

39082107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119743558-G-A

39082107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119743558-G-T

39082117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119743568-A-G

39083997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119745638-G-A

39084008-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119745649-T-A

http://identifiers.org/hco/3/GRCh38#39084130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#119745772-C-A

39084130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119745772-C-T

39084347-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119745979-T-A

39084347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119745979-T-C

39084543-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119746083-T-A

39084543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119746083-T-C

39085745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119747739-T-C

39088047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119748649-G-A

39088114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119748700-G-A

39088137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 119748724-A-G

39088195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 119748782-C-T

39088318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119748888-T-C

39088357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119748900-A-G

39088635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119749206-G-A

39088703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119749273-G-A

39088821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119749367-G-T

39089101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119749529-A-G

39089101-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119749529-A-T

39089131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119749545-T-C

39089140-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119749554-A-T

39089150-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119749564-T-A

39089240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 119749632-C-T

http://identifiers.org/hco/3/GRCh38#39089425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#119749788-C-A

39089426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119749789-A-G

http://identifiers.org/hco/3/GRCh38#39089457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#119749827-C-A

39089470-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119749840-A-T

39089542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119749916-A-G

39089543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119749917-C-T

http://identifiers.org/hco/3/GRCh38#39089574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#119749948-C-A

http://identifiers.org/hco/3/GRCh38#39089681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#119750036-C-A

http://identifiers.org/hco/3/GRCh38#39089734-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#119750089-A-C

39089907-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119750224-T-G

39089944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119750259-A-G

39090034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119750349-G-A

39090034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119750349-G-T

39090058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119750372-C-T

39090062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119750376-C-T

39090068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119750382-G-T

http://identifiers.org/hco/3/GRCh38#39090092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#119750401-C-A

39090092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119750401-C-T

39090108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119750416-A-G

39090176-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119750462-G-C

39090218-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119750503-T-G

39090292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119750573-A-G

http://identifiers.org/hco/3/GRCh38#39090295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#119750576-C-A

39090295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119750576-C-T

39090313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119750593-T-C

39090404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119750681-T-C

39090478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119750747-T-C

39090560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119750792-T-C

39090593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119750825-G-A

39090593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119750825-G-T

39090653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119750880-A-G

http://identifiers.org/hco/3/GRCh38#39090682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#119750907-C-A

http://identifiers.org/hco/3/GRCh38#39090722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#119750949-C-A

39090766-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119750990-T-G

39090830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119751055-G-T

39090856-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119751081-T-A

39090856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119751081-T-C

39090884-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119751108-T-A

http://identifiers.org/hco/3/GRCh38#39090939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#119751160-C-A

http://identifiers.org/hco/3/GRCh38#39091216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#119751303-C-A

39091216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119751303-C-T

39091258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119751340-G-A

39091258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119751340-G-T

39091279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119751361-G-A

39091279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119751361-G-T

39091414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119751453-A-G

http://identifiers.org/hco/3/GRCh38#39091515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#119751578-C-A

http://identifiers.org/hco/3/GRCh38#39091721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#119751781-C-A

39091721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119751781-C-T

39091724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119751784-G-A

39091724-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119751784-G-C

39091737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119751796-A-G

39091940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119751943-G-A

39092419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119752269-A-G

39092614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119752399-C-T

39092672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119752443-G-T

39092834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119752591-G-A

http://identifiers.org/hco/3/GRCh38#39093728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#119753014-C-A

39093745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119753030-G-A

39093745-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119753030-G-C

39093745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119753030-G-T

http://identifiers.org/hco/3/GRCh38#39093779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#119753070-C-A

39093836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119753115-T-C

39094084-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119753346-C-G

39094139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119753381-T-C

39094141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119753383-G-T

39094143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119753385-G-A

39094143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119753385-G-T

39094217-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119753452-T-A

39094230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119753465-A-G

39094230-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119753465-A-T

http://identifiers.org/hco/3/GRCh38#39094457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#119753626-C-A

39094460-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119753629-A-T

http://identifiers.org/hco/3/GRCh38#39094490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#119753645-C-A

39094539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119753683-T-C

39094574-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119753712-G-C

http://identifiers.org/hco/3/GRCh38#39094578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#119753716-C-A

39094578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119753716-C-T

39094783-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 119753910-C-G

39094783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 119753910-C-T

http://identifiers.org/hco/3/GRCh38#39095035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#119754132-C-A

39095035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 119754132-C-T

39095125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 119754219-T-C

http://identifiers.org/hco/3/GRCh38#39095135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#119754229-C-A

39095135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 119754229-C-T

http://identifiers.org/hco/3/GRCh38#39095218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#119754312-C-A

39095218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 119754312-C-T

39096093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 119755160-G-A

39096633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30914
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 119755621-A-G