48618349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88976809-A-G

http://identifiers.org/hco/2/GRCh38#48618413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#88976867-C-A

48618413-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88976867-C-G

48618413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88976867-C-T

48618724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88977130-T-C

48618724-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88977130-T-G

48618733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88977139-A-G

48618774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88977190-T-C

48618840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88977280-T-C

48618872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88977311-T-C

48618945-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88977404-G-C

48619018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88977475-A-G

48619597-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88977665-C-G

48619684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88977743-C-T

48619706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88977764-G-A

48619829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88978043-A-G

48620396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88978503-C-T

48620865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88978636-A-G

48620892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88978663-A-G

48620987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88978750-T-C

48621069-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88978816-T-G

48621072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88978818-G-T

48621224-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88978984-A-T

48621251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88979011-T-C

48621274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88979034-A-G

48621294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 88979051-G-A

http://identifiers.org/hco/2/GRCh38#48621343-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#88979089-A-C

48621601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88979607-G-T

48621725-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88979803-A-T

48621729-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88979807-T-G

48621731-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88979809-G-C

48621743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88979821-G-T

48621748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88979826-C-T

http://identifiers.org/hco/2/GRCh38#48621878-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#88979959-A-C

http://identifiers.org/hco/2/GRCh38#48621914-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#88979990-A-C

48621914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88979990-A-G

http://identifiers.org/hco/2/GRCh38#48621982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#88980071-C-A

http://identifiers.org/hco/2/GRCh38#48622988-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#88983002-A-C

48637266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88995331-G-A

48637294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88995356-A-G

48640959-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88995666-T-G

48641141-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88995824-T-G

48641165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88995842-T-C

48641194-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88995871-C-G

48642149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88997097-A-G

48642231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88997176-G-T

48642325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88997270-A-G

48642325-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88997270-A-T

48642363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88997377-A-G

48642375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88997389-T-C

48642392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88997405-T-C

48642392-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88997405-T-G

48642406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88997419-A-G

48642407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88997420-T-C

48642407-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88997420-T-G

48642448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88997461-A-G

48642455-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 88997468-C-G

48642492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88997480-A-G

48642537-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88997521-T-A

48642537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88997521-T-C

http://identifiers.org/hco/2/GRCh38#48642982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#88997603-C-A

48643067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88997685-A-G

48643067-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88997685-A-T

48643080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88997698-G-A

48643470-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88998055-T-G

48643527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88998106-C-T

48644374-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88998371-C-G

48644374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88998371-C-T

48644401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88998393-T-C

http://identifiers.org/hco/2/GRCh38#48644404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#88998396-C-A

48644404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88998396-C-T

48644635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88998642-A-G

48644978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88999092-A-G

http://identifiers.org/hco/2/GRCh38#48645011-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#88999124-A-C

http://identifiers.org/hco/2/GRCh38#48645223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#88999436-C-A

48645223-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88999436-C-G

48645242-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88999618-T-A

48645242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88999618-T-C

48645281-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88999657-A-T

48645310-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88999686-G-C

48645351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88999727-G-A

48646424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89001502-A-G

48646424-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89001502-A-T

48646662-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: missense variant
orthologous variants: 89001740-C-G

48646662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: synonymous variant
orthologous variants: 89001740-C-T

48646669-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: missense variant
orthologous variants: 89001747-C-G

48646669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: missense variant
orthologous variants: 89001747-C-T

http://identifiers.org/hco/2/GRCh38#48646705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#89001783-C-A

48646710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: missense variant
orthologous variants: 89001788-G-A

48646763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: synonymous variant
orthologous variants: 89001817-G-A

48646892-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: missense variant
orthologous variants: 89001946-T-G

48646917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: missense variant
orthologous variants: 89001971-G-A

48646917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: missense variant
orthologous variants: 89001971-G-T

48647007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: missense variant
orthologous variants: 89002061-A-G

http://identifiers.org/hco/2/GRCh38#48647029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#89002083-C-A

48647029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: missense variant
orthologous variants: 89002083-C-T

48647048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89002102-G-A

48647053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89002107-G-A

48647053-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89002107-G-C

48647053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89002107-G-T

48648314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89002990-A-G

48648426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89003100-T-C

48668376-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89016982-C-G

48668376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89016982-C-T

http://identifiers.org/hco/2/GRCh38#48668485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#89017089-C-A

48669156-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89018337-C-G

48669254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89018432-G-A

48669439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89018591-C-T

48669448-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89018600-T-A

48669539-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89018687-T-A

48669584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89018727-A-G

48669613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89018756-G-A

48669613-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89018756-G-C

http://identifiers.org/hco/2/GRCh38#48669629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#89018772-C-A

48669629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89018772-C-T

48669635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89018778-T-C

48669713-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89018860-T-A

48669713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89018860-T-C

48669740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: missense variant
orthologous variants: 89018887-G-A

48669740-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: missense variant
orthologous variants: 89018887-G-C

48669740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: missense variant
orthologous variants: 89018887-G-T

48669753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: missense variant
orthologous variants: 89018900-G-A

48669753-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: missense variant
orthologous variants: 89018900-G-C

48669753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: missense variant
orthologous variants: 89018900-G-T

48669799-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: missense variant
orthologous variants: 89018946-C-G

48669799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: synonymous variant
orthologous variants: 89018946-C-T

48669802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: synonymous variant
orthologous variants: 89018949-T-C

http://identifiers.org/hco/2/GRCh38#48669814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#89018961-C-A

48671508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89019702-T-C

http://identifiers.org/hco/2/GRCh38#48671509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#89019703-C-A

48671509-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89019703-C-G

48671509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89019703-C-T

48671532-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89019724-A-T

48671764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89019956-A-G

http://identifiers.org/hco/2/GRCh38#48671771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#89019963-C-A

48671771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89019963-C-T

http://identifiers.org/hco/2/GRCh38#48671941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#89021174-C-A

48672055-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89021257-A-T

http://identifiers.org/hco/2/GRCh38#48672068-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#89021268-A-C

48672107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89021306-A-G

48672192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89021393-A-G

48672255-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89021455-G-C

http://identifiers.org/hco/2/GRCh38#48679193-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#89022193-A-C

48679193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89022193-A-G

http://identifiers.org/hco/2/GRCh38#48679256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#89022242-C-A

48679256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89022242-C-T

48679258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89022244-A-G

48679286-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89022271-T-A

48679436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 89022411-G-A

http://identifiers.org/hco/2/GRCh38#48679461-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#89022436-A-C

48679461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89022436-A-G

48679461-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89022436-A-T

48679465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89022440-A-G

48679465-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89022440-A-T

48679467-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89022446-T-A

48679474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89022453-A-G

48679519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89022505-G-A

48679519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89022505-G-T

48679520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89022506-A-G

48679520-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89022506-A-T

48679664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89022638-A-G

http://identifiers.org/hco/2/GRCh38#48681806-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#89023008-A-C

48681806-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89023008-A-T

http://identifiers.org/hco/2/GRCh38#48681822-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#89023024-A-C

48681855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89023056-A-G

48682807-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89043334-C-G

48682872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89043400-T-C

48682899-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89043427-C-G

48683017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89043544-G-T

48683155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89043682-C-T

48683278-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89044608-A-T

48683296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89044626-A-G

48683409-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89044741-T-A

48683552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89044868-C-T

48683721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89044991-G-A

48683809-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89045071-G-C

48683944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89045158-G-A

48683944-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89045158-G-C

48683948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89045162-C-T

48683949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89045163-A-G

48684219-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89045284-G-C

48684243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89045297-G-T

48684550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89045533-G-A

http://identifiers.org/hco/2/GRCh38#48684620-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#89045600-A-C

48685378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89046844-G-T

48685381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89046847-T-C

48685551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89047002-G-A

48685561-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89047005-C-G

48685747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89047207-C-T

48685758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89047218-A-G

48685762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89047222-A-G

48686052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89047446-G-A

48686062-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89047454-T-A

48686379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89047900-A-G

48686450-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89047956-T-A

48686450-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89047956-T-G

48686707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89048203-A-G

48686715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89048211-C-T

48686724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89048219-T-C

48686781-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89048273-T-A

http://identifiers.org/hco/2/GRCh38#48686842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#89048685-C-A

48686922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89048757-G-A

48686922-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89048757-G-T

48686961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89048786-C-T

48686962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89048787-G-A

48686964-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89048789-G-C

48687244-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89049005-T-G

48687285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89049046-T-C

48687286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89049047-G-T

48687334-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89049091-G-C

48687334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89049091-G-T

48687358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89049113-A-G

48687397-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89049161-A-T

48687428-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89049200-T-G

http://identifiers.org/hco/2/GRCh38#48687513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#89049272-C-A

http://identifiers.org/hco/2/GRCh38#48687585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#89049322-C-A

48687653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89049393-A-G

48687674-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89049414-T-A

48687707-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 89049440-G-C

48687747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 89049463-G-A

48687747-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 89049463-G-C

http://identifiers.org/hco/2/GRCh38#48687802-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#89049518-A-C

48687802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 3_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 89049518-A-G

48687885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 3_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 89049601-G-A

48688009-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 3_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 89049725-T-A

48688048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 3_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 89049764-T-C

http://identifiers.org/hco/2/GRCh38#48688271-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#89049987-A-C

48688271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 89049987-A-G

48688271-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 89049987-A-T

48688335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 89050051-G-A

48688796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, missense_variant
orthologous variants: 89050512-C-T

48688822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 89050538-T-C

48688879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89050600-G-A

48688883-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89050604-T-G

48688884-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89050605-T-G

48688966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89050703-G-T

http://identifiers.org/hco/2/GRCh38#48689366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#89050943-C-A

http://identifiers.org/hco/2/GRCh38#48689389-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#89050962-A-C

48689425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89050997-T-C

48689507-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89051078-C-G

48689507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89051078-C-T

48691171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89054013-A-G

48691227-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89054062-A-T

48691518-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89054316-T-A

48691518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89054316-T-C

48691531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89054329-A-G

48691891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89054367-C-T

48691957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89054432-G-A

48692079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89054543-T-C

48692420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89054837-C-T

http://identifiers.org/hco/2/GRCh38#48692649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#89054992-C-A

48692649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89054992-C-T

48692650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89054993-A-G

48692690-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89055048-G-C

48692712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89055070-G-A

48692728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89055089-C-T

48692729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89055090-T-C

48692901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89055437-T-C

48692949-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89055455-T-G

48692968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89055472-T-C

48693023-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89055523-C-G

48693023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89055523-C-T

48693052-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89055546-C-G

http://identifiers.org/hco/2/GRCh38#48693072-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#89055566-A-C

48693092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89055586-G-T

48693162-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89055651-G-C

48693358-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89055830-A-T

48693457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89055953-T-C

48693569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89056056-C-T

48693934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89057224-T-C

48693935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89057225-G-A

48693935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89057225-G-T

http://identifiers.org/hco/2/GRCh38#48693955-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#89057245-A-C

48694076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89057381-A-G

48694092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89057396-A-G

http://identifiers.org/hco/2/GRCh38#48694174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#89057483-C-A

48694174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89057483-C-T

48694190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89057499-C-T

48694381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89057690-T-C

48694388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 89057697-A-G

48694388-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 89057697-A-T

48694412-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89057721-C-G

48694412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89057721-C-T

48694419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89057728-T-C

http://identifiers.org/hco/2/GRCh38#48694420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#89057729-C-A

48694420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89057729-C-T

48694545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89057854-A-G

48694572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89057888-A-G

48694646-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89057966-C-G

48694733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89058048-T-C

48694752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89058065-A-G

48694798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89058108-G-A

48696893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89059393-T-C

48697019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89059543-A-G

48697158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89059694-A-G

48697240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89059765-T-C

48697303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89059854-A-G

http://identifiers.org/hco/2/GRCh38#48697411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#89059983-C-A

48697587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89060230-G-A

48697669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89060339-G-A

48698007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89060650-A-G

48698050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89060718-C-T

48698184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89060848-T-C

48698473-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89061070-T-A

48698473-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89061070-T-G

48698572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89061135-C-T

48698601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89061158-T-C

48698674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 89061231-C-T

48698816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89061373-G-A

48698841-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89061398-T-G

48699319-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89061560-T-A

48699357-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89061598-C-G

48699363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89061612-C-T

48699406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89061668-C-T

48699551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89061808-T-C

48699612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89061870-C-T

http://identifiers.org/hco/2/GRCh38#48699649-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#89061906-A-C

48699658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, undefined
orthologous variants: 89061915-G-A

48699748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89061967-C-T

48699982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89062197-G-T

48700050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89062268-G-T

48708272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89062712-G-T

48708353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89062796-C-T

48708913-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 89062944-T-A

48708913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 89062944-T-C

48708914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 89062945-G-T

48708923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 89062954-G-T

48708979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 89063010-C-T

48708984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 89063015-T-C

48708984-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 89063015-T-G

http://identifiers.org/hco/2/GRCh38#48709058-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#89063095-A-C

48709058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89063095-A-G

48709094-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89063129-T-G

http://identifiers.org/hco/2/GRCh38#48709148-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#89063164-A-C

48709211-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89063218-G-C

48709294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89063298-C-T

48709386-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89063387-C-G

http://identifiers.org/hco/2/GRCh38#48709542-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#89063518-A-C

48709542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89063518-A-G

48711848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89063635-G-A

48711965-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89063683-T-G

48712068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89063783-C-T

48712069-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89063784-C-G

http://identifiers.org/hco/2/GRCh38#48712155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#89063866-C-A

48712243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89063945-T-C

48712282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89063984-G-T

48712300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89064002-G-T

http://identifiers.org/hco/2/GRCh38#48712325-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#89064034-A-C

48712405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89064102-G-A

48712405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89064102-G-T

http://identifiers.org/hco/2/GRCh38#48712746-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#89064312-A-C

48712931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89064501-T-C

48712945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89064515-G-A

48713016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89064566-G-A

48713162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89064705-G-A

48713162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89064705-G-T

48713163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89064706-T-C

48713167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89064710-T-C

48713239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89064996-T-C

48713279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89065036-T-C

48713364-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89065113-C-G

48713384-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89065132-C-G

48713384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89065132-C-T

48713532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89065331-G-T

48713695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89065478-G-A

48713695-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89065478-G-C

48713947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89065732-A-G

48714105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89065894-G-T

48714205-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89066046-T-A

48714240-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89066077-A-T

48714241-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89066078-C-G

48714425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89066297-T-C

48714485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89066346-T-C

48714522-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89066377-C-G

48714522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89066377-C-T

48714760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89066639-C-T

48714776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89066659-C-T

48715708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89066939-C-T

48716804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89067682-C-T

48716840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89067717-G-A

http://identifiers.org/hco/2/GRCh38#48716863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#89067740-C-A

48716863-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89067740-C-G

48717067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89067876-T-C

48717113-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89067903-C-G

48717113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89067903-C-T

48717163-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89067948-G-C

48717163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89067948-G-T

48717407-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89068432-C-G

48717450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89068482-C-T

48717582-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89068561-C-G

48717582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89068561-C-T

48717693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89068669-G-A

48718025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89068964-C-T

48718174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89069057-C-T

48718563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89069389-C-T

48718621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89069467-T-C

48718703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89069531-C-T

48718922-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89069728-T-G

48718969-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89069776-T-A

48718969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89069776-T-C

48719351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89071100-C-T

48719380-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89071129-T-A

48719496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89071229-G-T

http://identifiers.org/hco/2/GRCh38#48719567-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#89071302-A-C

48719567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89071302-A-G

48719585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89071332-T-C

48720031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89071770-A-G

48720031-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89071770-A-T

48720064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89071802-G-A

48720282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89071986-T-C

48720355-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89072041-A-T

48720376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89072063-C-T

48720396-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89072083-G-C

48720402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89072089-G-T

48723357-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89072308-T-G

48723361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89072312-G-T

48723403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89072356-G-A

48723403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89072356-G-T

48723415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89072368-G-T

48723470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 89072424-A-G

48723518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 89072472-G-A

48723648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 89072602-G-A

48723718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89072672-T-C

48723745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89072695-G-A

48723745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89072695-G-T

48723752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89072702-A-G

48723761-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89072711-T-G

48723785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89072734-G-A

48723785-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89072734-G-C

48723785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89072734-G-T

48723807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89072756-A-G

48724307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89073236-G-A

48724326-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89073255-T-A

48724326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89073255-T-C

48724354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89073283-G-A

48724820-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89073736-C-G

48724884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89073800-A-G

48724948-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89073929-G-C

48725611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89074612-T-C

48725642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89074645-C-T

48725648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89074651-C-T

48725760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89074765-G-A

48725760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89074765-G-T

48725781-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89074785-T-A

48725781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89074785-T-C

48725816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: -A-G

http://identifiers.org/hco/2/GRCh38#48725869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#89074861-C-A

48725869-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89074861-C-G

48725884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89074875-G-A

48725977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89074957-G-T

48726122-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89075104-C-G

http://identifiers.org/hco/2/GRCh38#48726139-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#89075120-A-C

48726249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89075228-C-T

48726765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89075443-G-T

48726783-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: -T-A

48726793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: -G-A

48726914-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89075535-C-G

48726941-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89075562-T-G

48727491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89075911-C-T

48727575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89075960-T-C

48727679-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89076056-C-G

48727850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89076235-C-T

48727925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89076308-G-A

http://identifiers.org/hco/2/GRCh38#48728243-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#89076390-A-C

48728250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89076397-C-T

48728361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89076504-G-T

48728374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89076517-T-C

48728385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89076527-T-C

48728510-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89076638-C-G

48728687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89076787-C-T

48728863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89076973-C-T

48729013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89077125-G-A

48729013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89077125-G-T

48729040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89077152-G-T

48729064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89077176-A-G

48729112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89077224-A-G

48729131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89077243-C-T

http://identifiers.org/hco/2/GRCh38#48729376-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#89077476-C-A

48729376-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89077476-C-G

48729376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89077476-C-T

48729630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89077706-G-A

48729771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89077851-C-T

48729809-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89077886-T-A

48729816-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89077893-T-G

48730211-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89078257-A-T

48730241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89078283-A-G

48730246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89078288-T-C

48730263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89078305-A-G

48730434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89078640-A-G

48730442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89078648-A-G

http://identifiers.org/hco/2/GRCh38#48730501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#89078713-C-A

48730512-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89078724-A-T

48730513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89078725-T-C

48730540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89078752-A-G

48730575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89078786-T-C

48730668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89078887-G-A

48730668-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89078887-G-C

48730841-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89079054-G-C

48730905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89079117-A-G

48730952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89079163-A-G

48731095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89079306-G-T

http://identifiers.org/hco/2/GRCh38#48731167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#89079379-C-A

48731167-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89079379-C-G

48731167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89079379-C-T

48731199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89079412-G-A

48731199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89079412-G-T

48731280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 89079493-A-G

48731337-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89079544-A-T

48731362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89079569-G-T

48731371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89079579-G-A

48731371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89079579-G-T

48731650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89079916-A-G

48731650-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89079916-A-T

48731679-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89079937-A-T

48731704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89079946-C-T

48731709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89079951-C-T

48731859-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89080107-A-T

http://identifiers.org/hco/2/GRCh38#48731865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#89080113-C-A

48731906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89080166-A-G

48731906-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89080166-A-T

48731933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89080190-C-T

http://identifiers.org/hco/2/GRCh38#48731948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#89080203-C-A

48731948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89080203-C-T

48732116-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89080367-A-T

48732253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89080476-G-T

48732368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89080884-G-A

48732409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89080926-T-C

48732423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89080933-C-T

48732461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89080971-A-G

48732512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89081026-A-G

48732615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89081129-T-C

48732808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89081284-A-G

48732852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron variant
orthologous variants: 89081327-A-G

48732899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, missense_variant
orthologous variants: 89081375-C-T

48732912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, missense_variant
orthologous variants: 89081388-C-T

48732913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30727
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 89081389-G-A