116910988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 118293494-G-A

116910988-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 118293494-G-C

116910988-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 118293494-G-T

http://identifiers.org/hco/12/GRCh38#116911021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#118293461-C-A

116911021-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 118293461-C-G

116911021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 118293461-C-T

116911082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 118293400-G-A

116911082-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 118293400-G-C

116911082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 118293400-G-T

http://identifiers.org/hco/12/GRCh38#116911149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118293333-C-A

116911149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118293333-C-T

116911270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 118293209-A-G

116911272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 118293207-G-A

116911272-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 118293207-G-C

116911272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 118293207-G-T

116911306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 118293173-A-G

116911676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118292903-C-T

116911686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118292874-A-G

http://identifiers.org/hco/12/GRCh38#116911757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118292808-C-A

116918057-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118287938-T-G

116918260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118287756-C-T

116918306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118287716-G-A

116918567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118287447-A-G

116920667-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118286097-C-G

116920981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118285598-G-A

116921199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118285282-G-A

116921291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118285203-A-G

116922173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118284719-C-T

116922310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118284615-G-A

116922693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118284281-A-G

116925538-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118283083-T-G

116926469-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118282126-T-A

116926512-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118282090-T-A

116926886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118281752-G-A

116926934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118281709-G-A

116927230-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118281449-C-G

116927333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118281351-T-C

116927529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118281220-A-G

116927769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118281026-A-G

http://identifiers.org/hco/12/GRCh38#116927890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118280948-C-A

116927890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118280948-C-T

http://identifiers.org/hco/12/GRCh38#116927894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118280944-C-A

116927894-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118280944-C-G

116928002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118280852-T-C

116928002-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118280852-T-G

116928006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118280848-T-C

116928030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118280828-T-C

116928055-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118280803-C-G

116928113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118280745-G-A

116928114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118280744-G-A

116928133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118280725-G-A

116928133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118280725-G-T

http://identifiers.org/hco/12/GRCh38#116928143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118280716-C-A

116928143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118280716-C-T

116928255-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118280557-T-A

116928255-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118280557-T-G

116928416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118280433-A-G

116928595-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118280273-C-G

116928663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118280211-C-T

116929206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118279583-C-T

116933097-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118278942-C-G

116933221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118278849-G-A

116933224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118278846-G-A

116933331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118278755-A-G

116934378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118277775-A-G

http://identifiers.org/hco/12/GRCh38#116934738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118277089-C-A

116934747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118277075-A-G

116934939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118276893-C-T

116935344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118276441-T-C

http://identifiers.org/hco/12/GRCh38#116935715-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118276192-A-C

http://identifiers.org/hco/12/GRCh38#116937658-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118274818-A-C

116937661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118274815-G-A

116937702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118274793-G-A

116937885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118274646-G-A

116938187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118274376-T-C

116939381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118273717-G-A

116939465-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118273644-T-A

116939499-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118273614-A-T

116939961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118273190-T-C

116940183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118272973-G-T

116940194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118272963-G-A

116940268-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118272900-T-A

http://identifiers.org/hco/12/GRCh38#116940291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118272879-C-A

116940380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118272792-A-G

116940380-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118272792-A-T

116944506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118267799-G-A

116944578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118267731-C-T

116944586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118267725-C-T

116944599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118267712-G-A

116944793-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118267573-G-C

116944797-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118267569-T-A

116945218-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118267176-T-G

http://identifiers.org/hco/12/GRCh38#116945227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118267170-C-A

116945227-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118267170-C-G

116945227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118267170-C-T

116945305-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118267093-A-T

116945680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118266743-A-G

116946278-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118266175-G-C

116947142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118265460-G-A

116947867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118265114-A-G

116947912-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118265065-C-G

116947920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118265057-C-T

116947995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118265009-G-A

116947995-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118265009-G-C

116948013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118264991-G-A

116948024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118264980-C-T

http://identifiers.org/hco/12/GRCh38#116949330-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118263345-A-C

116949331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118263344-G-A

116949331-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118263344-G-T

http://identifiers.org/hco/12/GRCh38#116949334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118263341-C-A

116949381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118263292-T-C

http://identifiers.org/hco/12/GRCh38#116949397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118263277-C-A

116949409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118263262-G-T

116949480-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118263212-A-T

116949490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118263203-G-T

116949510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118263191-G-T

116949512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118263189-C-T

http://identifiers.org/hco/12/GRCh38#116949530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118263171-C-A

116949530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118263171-C-T

116949535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118263166-G-A

116949535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118263166-G-T

116949553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118263145-A-G

116949569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118263134-G-A

116949569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118263134-G-T

116949582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118263121-A-G

116950081-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118262893-T-A

116950660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118262090-G-T

116950704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118262046-A-G

116950779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118261923-C-T

116950780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118261922-G-A

116950780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118261922-G-T

116950968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118261706-G-A

http://identifiers.org/hco/12/GRCh38#116950997-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118261681-A-C

116951086-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118261600-G-T

116951133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118261553-A-G

116951219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118261470-G-A

116951660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118261092-G-A

116951803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118260995-A-G

116955006-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118259705-T-A

116955011-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118259700-T-G

116955114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118259606-G-T

116955119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118259600-G-A

116955643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118259200-G-A

116955644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118259199-T-C

116955761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118258963-C-T

116955790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118258934-T-C

116956182-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118258525-C-G

116957463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118257774-G-A

116957872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118257436-T-C

116958293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118257020-A-G

116958510-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118256888-C-G

116959257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118255940-G-A

116959936-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118255316-T-A

116960006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118255254-A-G

116960151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118255114-C-T

116960429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118254899-C-T

116962117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118254410-C-T

116962180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118254350-T-C

116962282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118254219-C-T

116962435-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118254081-G-C

116963059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118253595-A-G

116963460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118253213-C-T

http://identifiers.org/hco/12/GRCh38#116963595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118253090-C-A

http://identifiers.org/hco/12/GRCh38#116963981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118252550-C-A

116964149-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118252433-C-G

116964349-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118252270-T-A

http://identifiers.org/hco/12/GRCh38#116964498-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118252025-A-C

http://identifiers.org/hco/12/GRCh38#116964823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118251706-C-A

116964882-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118251626-T-A

http://identifiers.org/hco/12/GRCh38#116964883-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118251625-A-C

http://identifiers.org/hco/12/GRCh38#116964980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118251483-C-A

116964980-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118251483-C-G

116964980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118251483-C-T

116965132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118251326-A-G

116965161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118251297-G-A

116965215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118251243-A-G

116969388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118247330-C-T

116969645-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118247144-C-G

116969647-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118247142-G-C

116969819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118246983-A-G

116970402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118246415-G-A

116970402-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118246415-G-C

116970421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118246389-C-T

116970616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118246257-T-C

116970880-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118246020-A-T

116971009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118245928-T-C

116971075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118245871-G-A

116978327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118238567-G-T

116978338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118238556-G-A

http://identifiers.org/hco/12/GRCh38#116978344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118238553-C-A

116978427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118238469-T-C

116978715-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118238212-G-T

116978754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118238176-T-C

116979413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118237529-G-T

116979482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118237463-G-A

116979482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118237463-G-T

116979968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118237205-G-A

116980332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118236926-G-T

116982587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118234851-G-A

116983247-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118234383-C-G

116983257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118234373-T-C

116983260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118234370-A-G

116983635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118234090-G-A

http://identifiers.org/hco/12/GRCh38#116985172-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118233821-A-C

116985479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118233531-T-C

116985521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118233512-T-C

http://identifiers.org/hco/12/GRCh38#116985522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118233511-C-A

116985522-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118233511-C-G

116985548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118233485-A-G

116985555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118233479-A-G

http://identifiers.org/hco/12/GRCh38#116985560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118233474-C-A

116985595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118233442-G-A

http://identifiers.org/hco/12/GRCh38#116985604-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118233433-A-C

116985604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118233433-A-G

http://identifiers.org/hco/12/GRCh38#116985689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118232923-C-A

116985689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118232923-C-T

http://identifiers.org/hco/12/GRCh38#116986004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118232666-C-A

http://identifiers.org/hco/12/GRCh38#116986025-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118232642-A-C

116986025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118232642-A-G

http://identifiers.org/hco/12/GRCh38#116986666-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118232322-C-A

116986666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118232322-C-T

116986670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118232318-A-G

116986765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118232242-G-A

116986765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118232242-G-T

116987041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118231992-C-T

116987115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118231920-A-G

http://identifiers.org/hco/12/GRCh38#116987180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118231837-C-A

116987352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118231673-C-T

116987498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118231584-A-G

116987554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118231544-A-G

116987572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118231521-T-C

http://identifiers.org/hco/12/GRCh38#116987734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118231365-C-A

116988172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118231116-A-G

116988478-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118230901-C-G

116988720-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118230708-G-C

116992386-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118229229-A-T

116995977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118227695-C-T

116996104-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118227579-T-G

116996114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118227569-T-C

116996428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118227267-C-T

116996429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118227266-A-G

116998189-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118225959-T-G

116998194-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118225953-G-C

116998214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118225931-T-C

116998555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118225582-C-T

http://identifiers.org/hco/12/GRCh38#116998775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118225376-C-A

116998778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118225375-G-T

116999066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118225133-G-T

116999067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118225132-A-G

116999114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118225089-G-A

116999288-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118224896-C-G

http://identifiers.org/hco/12/GRCh38#116999303-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118224881-A-C

116999349-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118224838-C-G

116999449-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118224715-G-C

117000284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118224162-A-G

117000445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118224079-C-T

http://identifiers.org/hco/12/GRCh38#117000572-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118224010-A-C

117000572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118224010-A-G

117000954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118223692-T-C

117001288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118223424-G-A

117001288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118223424-G-T

117001298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118223413-C-T

117001345-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118223362-G-C

117001411-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118223305-C-G

117001611-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118223157-A-T

117001620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118223148-A-G

http://identifiers.org/hco/12/GRCh38#117001719-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118223048-A-C

117001731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118223036-A-G

117001782-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118223002-T-G

117001868-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118222959-C-G

117002036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118222874-T-C

117002447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118222494-G-T

117002562-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118222383-T-A

117002567-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118222378-G-C

117002729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118222220-G-T

117002915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118222052-G-A

117003067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118221948-G-A

117003266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118221803-C-T

http://identifiers.org/hco/12/GRCh38#117003297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118221657-C-A

117003297-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118221657-C-G

117003364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118221556-C-T

117003452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118221479-G-T

117003720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118221268-C-T

117003826-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118221157-T-A

117004414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118220621-C-T

117006378-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118219204-G-C

117006461-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118219144-T-G

117006548-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118219036-C-G

117006548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118219036-C-T

117010280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118215805-G-T

117010286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118215799-G-T

117010456-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron variant
orthologous variants: 118215632-T-G

117010596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron variant
orthologous variants: 118215544-A-G

117011347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron variant
orthologous variants: 118214850-A-G

117017468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron variant
orthologous variants: 118211981-T-C

117017522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron variant
orthologous variants: 118211931-A-G

117017532-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron variant
orthologous variants: 118211924-C-G

117017538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron variant
orthologous variants: 118211918-A-G

117017987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron variant
orthologous variants: 118211521-C-T

117018465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron variant
orthologous variants: 118211050-C-T

117018486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron variant
orthologous variants: 118211029-G-A

117018504-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron variant
orthologous variants: 118211011-C-G

117018504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron variant
orthologous variants: 118211011-C-T

117018858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron variant
orthologous variants: 118210734-G-A

117024101-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron variant
orthologous variants: 118208618-G-T

117024307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: missense variant
orthologous variants: 118208422-G-A

117027131-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron variant
orthologous variants: 118206984-A-T

117027339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron variant
orthologous variants: 118206826-G-A

117027361-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron variant
orthologous variants: 118206809-C-G

117027361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron variant
orthologous variants: 118206809-C-T

117027461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: missense variant
orthologous variants: 118206711-G-T

117027521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron variant
orthologous variants: 118206652-G-A

117027550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron variant
orthologous variants: 118206621-G-A

117027550-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron variant
orthologous variants: 118206621-G-T

http://identifiers.org/hco/12/GRCh38#117027555-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118206616-A-C

117027555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron variant
orthologous variants: 118206616-A-G

http://identifiers.org/hco/12/GRCh38#117027560-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118206614-A-C

117027560-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron variant
orthologous variants: 118206614-A-T

http://identifiers.org/hco/12/GRCh38#117027584-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118206592-A-C

117027584-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron variant
orthologous variants: 118206592-A-T

http://identifiers.org/hco/12/GRCh38#117027606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118206576-C-A

117027606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron variant
orthologous variants: 118206576-C-T

117027628-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron variant
orthologous variants: 118206554-T-A

117027628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron variant
orthologous variants: 118206554-T-C

http://identifiers.org/hco/12/GRCh38#117027897-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118206387-C-A

117027897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: intron variant
orthologous variants: 118206387-C-T

117028214-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: 3 prime UTR variant
orthologous variants: 118206119-C-G

117028214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: 3 prime UTR variant
orthologous variants: 118206119-C-T

117028269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: 3 prime UTR variant
orthologous variants: 118206062-G-A

117028269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13597
most severe consequence: 3 prime UTR variant
orthologous variants: 118206062-G-T