74871388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3 prime UTR variant
orthologous variants: 112174526-C-T

74871419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3 prime UTR variant
orthologous variants: 112174556-C-T

74871478-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3 prime UTR variant
orthologous variants: 112174615-T-G

74871505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3 prime UTR variant
orthologous variants: 112174642-G-A

74871616-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3 prime UTR variant
orthologous variants: 112174972-C-G

http://identifiers.org/hco/16/GRCh38#74871665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112175009-C-A

74871665-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3 prime UTR variant
orthologous variants: 112175009-C-G

74871665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3 prime UTR variant
orthologous variants: 112175009-C-T

74871666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3 prime UTR variant
orthologous variants: 112175010-A-G

74871672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3 prime UTR variant
orthologous variants: 112175016-G-T

74871687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3 prime UTR variant
orthologous variants: 112175031-G-A

74871687-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3 prime UTR variant
orthologous variants: 112175031-G-T

http://identifiers.org/hco/16/GRCh38#74871688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112175032-C-A

74871688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3 prime UTR variant
orthologous variants: 112175032-C-T

74871755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3 prime UTR variant
orthologous variants: 112175095-A-G

74871785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3 prime UTR variant
orthologous variants: 112175155-T-C

74871808-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3 prime UTR variant
orthologous variants: 112175176-G-C

74871808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3 prime UTR variant
orthologous variants: 112175176-G-T

74871814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3 prime UTR variant
orthologous variants: 112175182-T-C

74871814-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3 prime UTR variant
orthologous variants: 112175182-T-G

http://identifiers.org/hco/16/GRCh38#74871830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112175195-C-A

74871830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3 prime UTR variant
orthologous variants: 112175195-C-T

http://identifiers.org/hco/16/GRCh38#74871842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112175203-C-A

74871842-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3 prime UTR variant
orthologous variants: 112175203-C-G

74871842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3 prime UTR variant
orthologous variants: 112175203-C-T

74871843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3 prime UTR variant
orthologous variants: 112175204-G-A

74871843-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3 prime UTR variant
orthologous variants: 112175204-G-C

74871843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3 prime UTR variant
orthologous variants: 112175204-G-T

74871848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3 prime UTR variant
orthologous variants: 112175209-G-A

74871848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3 prime UTR variant
orthologous variants: 112175209-G-T

http://identifiers.org/hco/16/GRCh38#74871851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112175212-C-A

74871903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3 prime UTR variant
orthologous variants: 112175239-C-T

74871921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3 prime UTR variant
orthologous variants: 112175247-G-T

74871945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3 prime UTR variant
orthologous variants: 112175271-T-C

74871970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3 prime UTR variant
orthologous variants: 112175300-G-A

74871970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3 prime UTR variant
orthologous variants: 112175300-G-T

74872076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3 prime UTR variant
orthologous variants: 112175372-C-T

74872078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3 prime UTR variant
orthologous variants: 112175374-T-C

http://identifiers.org/hco/16/GRCh38#74872087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112175382-C-A

74872087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3 prime UTR variant
orthologous variants: 112175382-C-T

74873477-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3 prime UTR variant
orthologous variants: 112176568-G-C

74873477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3 prime UTR variant
orthologous variants: 112176568-G-T

74873585-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3 prime UTR variant
orthologous variants: 112176703-T-A

74873603-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3 prime UTR variant
orthologous variants: 112176721-A-T

74873607-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3 prime UTR variant
orthologous variants: 112176725-A-T

74873636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3 prime UTR variant
orthologous variants: 112176815-G-T

74873772-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3 prime UTR variant
orthologous variants: 112177029-A-T

http://identifiers.org/hco/16/GRCh38#74873815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112177071-C-A

74873815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3 prime UTR variant
orthologous variants: 112177071-C-T

http://identifiers.org/hco/16/GRCh38#74873875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112177146-C-A

74873875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3 prime UTR variant
orthologous variants: 112177146-C-T

74873900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3 prime UTR variant
orthologous variants: 112177172-C-T

74873901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3 prime UTR variant
orthologous variants: 112177173-T-C

http://identifiers.org/hco/16/GRCh38#74873969-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112177233-A-C

74873978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3 prime UTR variant
orthologous variants: 112177242-G-A

74873978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3 prime UTR variant
orthologous variants: 112177242-G-T

http://identifiers.org/hco/16/GRCh38#74873989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112177253-C-A

74873989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3 prime UTR variant
orthologous variants: 112177253-C-T

http://identifiers.org/hco/16/GRCh38#74874002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112177264-C-A

74874002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3 prime UTR variant
orthologous variants: 112177264-C-T

http://identifiers.org/hco/16/GRCh38#74874019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112177281-C-A

74874019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3 prime UTR variant
orthologous variants: 112177281-C-T

74874051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3 prime UTR variant
orthologous variants: 112177313-A-G

74874069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3 prime UTR variant
orthologous variants: 112177328-T-C

74874095-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 112177355-C-G

74874111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 112177371-G-T

http://identifiers.org/hco/16/GRCh38#74874227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112177494-C-A

74874227-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112177494-C-G

http://identifiers.org/hco/16/GRCh38#74874332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112177599-C-A

74874332-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112177599-C-G

74874332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112177599-C-T

74874350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112177617-G-A

http://identifiers.org/hco/16/GRCh38#74874365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112177632-C-A

74874365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112177632-C-T

74874465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112177732-G-A

74874473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112177740-A-G

74874525-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112177788-A-T

74874531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112177794-G-A

74874531-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112177794-G-C

74874531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112177794-G-T

74874534-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112177797-T-G

http://identifiers.org/hco/16/GRCh38#74874566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112177829-C-A

74874566-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112177829-C-G

74874566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112177829-C-T

74879658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112179919-G-A

74879824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112180107-G-A

74881969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112180975-T-C

http://identifiers.org/hco/16/GRCh38#74882078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112181231-C-A

74882082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112181235-T-C

74882087-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112181240-C-G

74882192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112181343-A-G

http://identifiers.org/hco/16/GRCh38#74885523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112185127-C-A

74885523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112185127-C-T

74885529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112185133-A-G

http://identifiers.org/hco/16/GRCh38#74885547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112185149-C-A

74885547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112185149-C-T

http://identifiers.org/hco/16/GRCh38#74885606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112185199-C-A

74885821-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112185408-G-C

74885821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112185408-G-T

74885834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112185421-A-G

74885835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112185422-G-A

74885835-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112185422-G-C

74886240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112185526-A-G

74886428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112185712-C-T

74886430-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112185714-A-T

74886432-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112185716-C-G

74886443-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112185732-T-A

74886443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112185732-T-C

74886445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112185734-G-A

74886445-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112185734-G-C

74886445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112185734-G-T

74886449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112185738-A-G

74886449-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112185738-A-T

74886466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112185755-T-C

74886543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron variant
orthologous variants: 112185835-A-G

74886784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron variant
orthologous variants: 112186017-G-A

74886827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron variant
orthologous variants: 112186059-G-A

74886842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron variant
orthologous variants: 112186079-G-A

74886842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron variant
orthologous variants: 112186079-G-T

74886866-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron variant
orthologous variants: 112186101-T-A

74886905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron variant
orthologous variants: 112186132-G-A

74887136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron variant
orthologous variants: 112186375-T-C

74887328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron variant
orthologous variants: 112187008-T-C

74887564-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron variant
orthologous variants: 112187145-T-A

74887564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron variant
orthologous variants: 112187145-T-C

74887564-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron variant
orthologous variants: 112187145-T-G

74887570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron variant
orthologous variants: 112187151-G-A

74887570-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron variant
orthologous variants: 112187151-G-C

74887570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron variant
orthologous variants: 112187151-G-T

74887580-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron variant
orthologous variants: 112187161-A-T

74887636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron variant
orthologous variants: 112187168-T-C

74887763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 112187293-A-G

74887763-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 112187293-A-T

74887764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron variant
orthologous variants: 112187294-G-T

74887766-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron variant
orthologous variants: 112187296-G-C

74887787-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron variant
orthologous variants: 112187310-T-A

74887787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron variant
orthologous variants: 112187310-T-C

74887790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron variant
orthologous variants: 112187313-C-T

74887794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron variant
orthologous variants: 112187317-A-G

74887848-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron variant
orthologous variants: 112187352-T-G

74888169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, splice_region_variant, synonymous_variant
orthologous variants: 112187394-A-G

74888184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 112187409-C-T

74888378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112187605-G-A

74888378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112187605-G-T

http://identifiers.org/hco/16/GRCh38#74888416-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112187639-A-C

74888417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112187640-G-A

74888417-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112187640-G-T

74888435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112187658-G-A

74888435-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112187658-G-C

74888435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112187658-G-T

74888459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112187681-G-A

74888463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112187685-T-C

74888475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112187697-C-T

74888585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112187785-G-A

http://identifiers.org/hco/16/GRCh38#74888609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112187808-C-A

74888664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112187876-T-C

74888692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112187914-A-G

74888747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112187970-G-A

74888751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112187974-C-T

74888760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112187983-C-T

74888773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112187994-C-T

74888842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112188030-G-A

74888892-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112188074-G-C

74888892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112188074-G-T

74888898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112188080-G-A

74888902-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112188084-G-C

74889016-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112188125-T-G

74889156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112188260-A-G

74889363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112188459-T-C

74889369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112188465-C-T

74889417-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112188513-G-C

74889520-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112188608-T-A

74889520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112188608-T-C

74889520-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112188608-T-G

http://identifiers.org/hco/16/GRCh38#74889582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112188670-C-A

74889582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112188670-C-T

74889605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112188691-G-A

74889605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112188691-G-T

74889606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112188692-G-A

74889606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112188692-G-T

74889691-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112188776-C-G

74889847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112188934-A-G

74889896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112188983-A-G

74889936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112189024-G-A

74889936-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112189024-G-C

74889936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112189024-G-T

74890472-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112189361-T-G

74890480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112189369-C-T

74890598-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112189482-C-G

74890672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112189541-C-T

74890781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112189640-C-T

http://identifiers.org/hco/16/GRCh38#74890818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112189671-C-A

74890818-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112189671-C-G

74891277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112189994-G-T

74891313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112190022-A-G

74891362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112190061-G-A

74891362-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112190061-G-C

74891371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112190070-A-G

74891377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112190077-G-A

74891377-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112190077-G-C

74891412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112190111-T-C

74891412-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112190111-T-G

http://identifiers.org/hco/16/GRCh38#74891550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112190208-C-A

74892344-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112192310-A-T

74892347-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112192313-G-T

74892369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112192335-T-C

74892471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112192408-G-A

74892523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112192460-G-A

74892523-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112192460-G-C

74892523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112192460-G-T

74892622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112192556-C-T

http://identifiers.org/hco/16/GRCh38#74892636-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112192570-A-C

http://identifiers.org/hco/16/GRCh38#74892846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112192745-C-A

74892902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112192785-G-A

74892906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112192788-C-T

74892976-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112192858-T-G

74892977-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112192859-G-C

74893528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112193296-G-A

74893528-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112193296-G-C

74893528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112193296-G-T

http://identifiers.org/hco/16/GRCh38#74893634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112193378-C-A

74893634-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112193378-C-G

74893634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112193378-C-T

74893648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112193389-G-A

74893648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112193389-G-T

74893650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112193396-G-A

74893650-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112193396-G-C

74893652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112193398-G-A

74893652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112193398-G-T

74893655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112193401-G-T

74893771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112193513-A-G

74893777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112193519-T-C

74893841-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112193582-T-A

74893841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112193582-T-C

74893940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112193682-T-C

74894359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112194098-A-G

74894456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112194196-C-T

74894620-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112194342-A-T

74894900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112194614-T-C

http://identifiers.org/hco/16/GRCh38#74894918-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112194632-A-C

74894930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112194642-A-G

74895026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112194709-C-T

74895892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112195157-G-T

74895946-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112195209-C-G

74895946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112195209-C-T

74895976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112195258-C-T

http://identifiers.org/hco/16/GRCh38#74895979-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112195261-A-C

74896052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112195351-T-C

http://identifiers.org/hco/16/GRCh38#74896306-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112195661-A-C

74896329-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112195680-C-G

74896919-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112195981-C-G

74897055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112196408-T-C

74897192-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112196521-T-G

74897275-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112196842-G-C

74897295-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112196862-G-C

74897463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112197069-T-C

74897668-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112197260-G-C

74897668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112197260-G-T

74897679-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112197271-T-G

74897809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112197444-C-T

74897841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112197466-T-C

74898022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112197651-T-C

74898300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112197927-T-C

74899055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112198625-C-T

74899380-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112198949-C-G

http://identifiers.org/hco/16/GRCh38#74899550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112199114-C-A

74899550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112199114-C-T

74899790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112199353-G-A

74899790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112199353-G-T

74899866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112199429-G-A

74899866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112199429-G-T

74900023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112199576-G-A

74900341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112199829-A-G

74900363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112199850-C-T

74900551-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112200041-T-G

74901890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112200560-G-A

74901890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112200560-G-T

74902216-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112200918-G-C

74903179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112201835-T-C

74903726-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112202456-G-C

74903758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112202485-A-G

74903813-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112202541-T-A

74903849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112202577-A-G

74903910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112202639-A-G

http://identifiers.org/hco/16/GRCh38#74903936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112202665-C-A

74904040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
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: 112202769-T-C

http://identifiers.org/hco/16/GRCh38#74904230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112202954-C-A

74908939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112205971-G-A

http://identifiers.org/hco/16/GRCh38#74909032-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112206056-A-C

74909129-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112206362-T-G

74909161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112206394-C-T

74909281-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112206445-C-G

http://identifiers.org/hco/16/GRCh38#74909355-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112206946-A-C

74909355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112206946-A-G

74909355-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112206946-A-T

74909388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112206963-G-T

74909402-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112206979-A-T

74909443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112207015-A-G

74909494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 112207068-G-A

74909494-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 112207068-G-C

74909494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 112207068-G-T

74909619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112207193-G-A

74909619-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112207193-G-C

74909619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112207193-G-T

74909787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112207353-A-G

74909945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112207511-A-G

74909949-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112207515-G-C

74909949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112207515-G-T

74910641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112207818-A-G

74910647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112207830-T-C

74912003-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112208300-A-T

74912098-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112208400-A-T

74912128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112208421-T-C

74912150-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 112208443-G-C

74912409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112208721-G-A

74912409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112208721-G-T

74912411-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112208723-C-G

74912414-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112208727-T-A

74912414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112208727-T-C

74912487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112208873-A-G

http://identifiers.org/hco/16/GRCh38#74912488-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112208874-A-C

74914313-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112210298-C-G

74914313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112210298-C-T

74914320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112210303-T-C

74914361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112210344-C-T

74914447-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112210428-G-C

74914997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112210680-A-G

74915979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112211831-G-A

74915981-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112211833-A-T

74916061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112211906-G-A

74916061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112211906-G-T

74916091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112211938-T-C

74916281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112212235-G-A

74916387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112212336-T-C

http://identifiers.org/hco/16/GRCh38#74916878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112212881-C-A

74916992-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112212990-T-A

74917064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112213071-A-G

74917116-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112213124-G-C

74917116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112213124-G-T

http://identifiers.org/hco/16/GRCh38#74917144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112213150-C-A

74917144-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112213150-C-G

74917258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112213235-G-A

74917409-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112213349-G-C

74917465-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112213414-G-C

74917977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112213596-G-A

74918012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 112213631-G-A

http://identifiers.org/hco/16/GRCh38#74918031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112213991-C-A

74918031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112213991-C-T

74918044-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112214004-C-G

74918067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112214028-G-A

74918067-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112214028-G-C

74918096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112214057-C-T

74918117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112214121-A-G

74918138-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112214141-A-T

74918197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112214197-G-A

74918294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112214285-T-C

74918295-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112214286-A-T

74918322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112214313-T-C

74918322-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112214313-T-G

74918466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112214433-T-C

74918472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112214439-C-T

74918646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112214620-G-A

74918652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112214626-T-C

74918678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112214651-C-T

74918719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112214690-G-A

74918861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112214835-T-C

74918861-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112214835-T-G

74918929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112214870-G-A

74918929-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112214870-G-C

http://identifiers.org/hco/16/GRCh38#74918947-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112214873-A-C

74918990-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112214910-T-G

74919024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112214945-G-T

74919256-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112215131-T-A

74919274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112215148-A-G

http://identifiers.org/hco/16/GRCh38#74921734-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112216716-A-C

74921828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112216796-C-T

74921856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112216834-G-T

74921868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112216842-G-T

http://identifiers.org/hco/16/GRCh38#74921897-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112216870-C-A

74921897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112216870-C-T

http://identifiers.org/hco/16/GRCh38#74922156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112217126-C-A

74922156-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112217126-C-G

74922156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112217126-C-T

74922160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112217130-G-A

74922469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112217692-C-T

74922855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112218045-G-A

74923041-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112218230-C-G

74923041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112218230-C-T

74923152-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112218354-T-G

74923851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112219289-A-G

74924020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112219413-A-G

74924025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112219418-C-T

74924056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112219490-T-C

74924105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112219629-A-G

74924133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112219657-A-G

74924133-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112219657-A-T

74924281-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112219789-G-C

74924431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112219926-T-C

http://identifiers.org/hco/16/GRCh38#74937263-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#112220389-C-A

74937291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112220414-C-T

74937309-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112220429-A-T

74937330-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112220443-G-C

74937409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112220519-T-C

http://identifiers.org/hco/16/GRCh38#74938020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112220741-C-A

74938020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112220741-C-T

74938028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112220749-G-A

74938028-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112220749-G-C

74938028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112220749-G-T

74938032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112220753-A-G

http://identifiers.org/hco/16/GRCh38#74938042-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112220762-A-C

http://identifiers.org/hco/16/GRCh38#74938043-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112220763-A-C

74938045-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112220765-T-A

74938045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112220765-T-C

74938045-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112220765-T-G

74938085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112220814-G-A

74938085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112220814-G-T

74938104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112220833-G-A

74938104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112220833-G-T

http://identifiers.org/hco/16/GRCh38#74938114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112220843-C-A

74938114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112220843-C-T

http://identifiers.org/hco/16/GRCh38#74938128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112220857-C-A

74938129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112220858-T-C

74938177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112220907-A-G

74938246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112220976-T-C

74938252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112220982-T-C

74938252-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112220982-T-G

74938309-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112221038-T-A

74938309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112221038-T-C

74938337-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112221071-G-C

74938337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112221071-G-T

74938357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112221089-G-A

74938477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112221196-G-A

74941801-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112221997-T-A

74941801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112221997-T-C

74942142-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112222351-G-C

74942300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112222474-T-C

74942332-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112222504-T-A

74942350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112222522-G-A

74942427-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112222599-G-C

74942712-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112223404-T-A

74942712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112223404-T-C

74942712-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112223404-T-G

74942738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 112223439-C-T

74942792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 112223493-A-G

74942844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112223546-G-A

74942844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112223546-G-T

74942860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112223562-C-T

http://identifiers.org/hco/16/GRCh38#74942861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112223563-C-A

74942861-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112223563-C-G

74942939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112223631-T-C

74942939-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112223631-T-G

74942952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112223644-G-A

74942952-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112223644-G-C

74942952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112223644-G-T

http://identifiers.org/hco/16/GRCh38#74948506-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112225191-A-C

74948577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112225262-A-G

74948578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112225263-T-C

http://identifiers.org/hco/16/GRCh38#74948604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112225290-C-A

74949631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112227589-G-A

74949631-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112227589-G-C

74949631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112227589-G-T

http://identifiers.org/hco/16/GRCh38#74949638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112227595-C-A

http://identifiers.org/hco/16/GRCh38#74949667-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112227622-A-C

74949667-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112227622-A-T

http://identifiers.org/hco/16/GRCh38#74949684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112227635-C-A

74949732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112227683-G-A

74949860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112227805-G-A

74949863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112227808-C-T

74949874-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112227819-A-T

74949875-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112227820-G-C

74949875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112227820-G-T

74949920-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112227861-T-A

74950406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112228450-T-C

http://identifiers.org/hco/16/GRCh38#74950604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112228591-C-A

74951301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112228948-C-T

74951490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112229146-G-A

74951490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112229146-G-T

74951575-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112229231-G-C

74951575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112229231-G-T

74951582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112229238-G-A

74951582-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112229238-G-C

74951582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112229238-G-T

74951597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112229260-G-T

74951614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112229277-G-T

74951631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112229294-A-G

http://identifiers.org/hco/16/GRCh38#74956227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112230538-C-A

74956227-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112230538-C-G

74956371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112230885-A-G

74956382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112230896-G-A

74956382-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112230896-G-C

74956382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112230896-G-T

74956428-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112230942-G-C

74956505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
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: 112230997-A-G

74956671-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112231161-G-C

74956750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112231234-G-A

74956832-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112231313-G-C

74956889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112231373-C-T

74956918-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112231403-C-G

74956957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112231421-C-T

74957428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112231570-C-T

74965450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112232228-C-T

74965491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112232268-A-G

74965630-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112232377-T-A

74965630-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112232377-T-G

74965649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112232396-A-G

74965655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112232402-G-A

74965655-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112232402-G-C

74965655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112232402-G-T

74965659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112232406-T-C

74965665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112232412-C-T

74965690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112232442-G-A

74965690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112232442-G-T

http://identifiers.org/hco/16/GRCh38#74965701-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112232453-A-C

74965701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112232453-A-G

74965814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112232565-C-T

74965835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112232586-A-G

http://identifiers.org/hco/16/GRCh38#74965841-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112232592-A-C

74965874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112232623-G-A

74965874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112232623-G-T

http://identifiers.org/hco/16/GRCh38#74965923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112232669-C-A

http://identifiers.org/hco/16/GRCh38#74965928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112232674-C-A

74965941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112232684-T-C

74967044-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112233767-G-C

74967214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112233933-G-A

http://identifiers.org/hco/16/GRCh38#74967253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112233972-C-A

74967414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112234120-G-A

74967499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112234206-C-T

74982463-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112243098-G-C

74982534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112243169-G-A

http://identifiers.org/hco/16/GRCh38#74982659-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112243293-A-C

74982870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112243507-T-C

74982931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112243562-T-C

74984134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112247784-G-A

74984140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112247791-G-T

http://identifiers.org/hco/16/GRCh38#74984683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112248262-C-A

74984683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112248262-C-T

http://identifiers.org/hco/16/GRCh38#74984709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#112248281-C-A

74984709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112248281-C-T

74984796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112248360-T-C

http://identifiers.org/hco/16/GRCh38#74984897-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#112248457-A-C

74984945-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112248526-C-G

http://identifiers.org/hco/16/GRCh38#74985009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#112248605-C-A

74985009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 112248605-C-T

http://identifiers.org/hco/16/GRCh38#74985031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#112248627-C-A

74985031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 112248627-C-T

http://identifiers.org/hco/16/GRCh38#74985037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112248632-C-A

74985037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112248632-C-T

74985148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112248754-G-A

74985148-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112248754-G-T

http://identifiers.org/hco/16/GRCh38#74985156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#112248762-C-A

http://identifiers.org/hco/16/GRCh38#74985212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#112248816-C-A

74985212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112248816-C-T

74985777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112249079-G-A

74985863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112249160-G-A

74985879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112249203-A-G

74986001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112249379-T-C

74986370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112249616-G-A

74986370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112249616-G-T

74986613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112249725-T-C

74987520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112250207-G-A

74987592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112250279-G-A

74989194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112253793-A-G

74989253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112253849-C-T

74989255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112253851-A-G

74989255-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112253851-A-T

74989312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112253895-A-G

74991541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112254137-G-A

http://identifiers.org/hco/16/GRCh38#74991665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112254259-C-A

74991786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112254909-C-T

74991976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112255083-T-C

74993120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112257014-T-C

74993138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112257032-G-A

74996659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

74996739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-T

74998273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112262322-C-T

74998394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112262444-A-G

74998394-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112262444-A-T

74998542-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112262576-C-G

74998560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112262641-C-T

74998583-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112262664-C-G

74998628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112262712-C-T

74998643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112262727-G-A

74998652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112262736-G-A

74998669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112262753-G-A

74998669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112262753-G-T

74998678-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112262762-G-C

74998680-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112262764-C-G

74998730-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112262817-C-G

74998798-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112262887-T-A

http://identifiers.org/hco/16/GRCh38#74998813-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#112262907-A-C

74998847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112262941-T-C

74998869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112262963-G-A

74998869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112262963-G-T

74998881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112262976-A-G

http://identifiers.org/hco/16/GRCh38#74998906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#112263006-C-A

74998906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112263006-C-T

74998934-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112263034-C-G

74998934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112263034-C-T

74998936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112263037-G-A

74998936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112263037-G-T

74998938-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112263039-C-G

http://identifiers.org/hco/16/GRCh38#74998961-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#112263062-A-C

74998961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112263062-A-G

http://identifiers.org/hco/16/GRCh38#74998974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112263075-C-A

74998974-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112263075-C-G

74998974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112263075-C-T

74998984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112263085-G-T

74998997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112263110-G-A

74998997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112263110-G-T

74998998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112263111-G-A

74998998-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112263111-G-C

74998998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112263111-G-T

http://identifiers.org/hco/16/GRCh38#74999050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112263163-C-A

74999050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112263163-C-T

74999054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112263167-G-A

74999054-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112263167-G-C

74999054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112263167-G-T

http://identifiers.org/hco/16/GRCh38#74999062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112263175-C-A

74999062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112263175-C-T

74999065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112263178-G-A

74999065-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112263178-G-C

74999065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112263178-G-T

74999075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112263188-G-T

74999082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112263195-C-T

74999119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112263236-G-A

74999192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112263311-G-A

74999202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112263321-C-T

74999205-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112263324-C-G

74999205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112263324-C-T

74999211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112263330-T-C

http://identifiers.org/hco/16/GRCh38#74999217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112263336-C-A

74999237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112263356-C-T

74999298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112263420-G-A

74999298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112263420-G-T

74999365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112263452-T-C

74999365-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112263452-T-G

74999367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112263454-G-A

74999367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112263454-G-T

http://identifiers.org/hco/16/GRCh38#74999373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#112263460-C-A

74999373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112263460-C-T

74999374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112263461-G-A

74999374-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112263461-G-C

74999374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112263461-G-T

74999531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112263618-T-C

74999531-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112263618-T-G

74999534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112263621-G-A

74999534-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112263621-G-T

74999536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112263623-T-C

74999536-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112263623-T-G

74999550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112263637-T-C

http://identifiers.org/hco/16/GRCh38#74999598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112263699-C-A

74999598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112263699-C-T

74999642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112263743-G-T

http://identifiers.org/hco/16/GRCh38#74999655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#112263756-C-A

74999655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112263756-C-T

74999719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 112263820-G-A

74999719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 112263820-G-T

75000162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 112264274-G-A

75000162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 112264274-G-T