79877447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105774867-T-C

79877578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105775000-G-T

79877659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105775046-A-G

79877825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105775202-C-T

http://identifiers.org/hco/13/GRCh38#79877851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105775229-C-A

79877908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105775273-A-G

79877966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105775363-C-T

79878079-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105775457-T-G

79878086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105775464-A-G

79878123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105775501-A-G

79878162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105775538-A-G

79878312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105775672-A-G

79878312-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105775672-A-T

http://identifiers.org/hco/13/GRCh38#79879995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105776406-C-A

http://identifiers.org/hco/13/GRCh38#79880038-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105776449-A-C

79880057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105776488-C-T

79880207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105776620-T-C

79880220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105776682-A-G

79880537-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105776886-A-T

79880647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105776992-C-T

79880790-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105777127-A-T

79880890-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105777235-G-C

79881041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105777394-C-T

http://identifiers.org/hco/13/GRCh38#79881129-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105777468-A-C

79881129-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105777468-A-T

79881131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105777470-A-G

79881134-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105777473-G-C

79881148-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105777487-C-G

79881148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105777487-C-T

79881150-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105777489-A-T

79881184-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105777523-A-T

79881267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105777608-T-C

79881291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105777633-T-C

79881313-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105777655-A-T

79881337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105777747-C-T

79881386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105777798-T-C

79881444-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105777857-A-T

79882294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105778635-G-A

79882294-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105778635-G-C

79882294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105778635-G-T

79883142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105778676-C-T

79883301-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105778836-G-C

79883360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105778890-A-G

79883469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105778988-C-T

79883707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105779180-G-A

79883771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105779222-G-A

79883820-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105779267-C-G

79883887-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105779334-A-T

79883932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105779374-G-A

79883967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105779411-G-A

79884327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105779695-G-A

79884458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105779800-G-A

79884463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105779805-A-G

79884573-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105779859-G-C

79884577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105779863-A-G

79884756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105780021-T-C

79884825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105780089-C-T

http://identifiers.org/hco/13/GRCh38#79884941-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105780204-A-C

79885030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105780294-A-G

79885260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105780528-C-T

79885268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105780536-A-G

79885321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105780590-C-T

79885345-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105780614-C-G

79885870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105780823-G-A

79885870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105780823-G-T

http://identifiers.org/hco/13/GRCh38#79885960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105780922-C-A

79886495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105781366-A-G

79886666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105781517-G-A

79897342-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105782209-A-T

79898328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105782756-A-G

79898462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105782873-A-G

79898491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105782907-C-T

79898663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105783077-C-T

79899118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105791499-C-T

79899162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105791545-A-G

79899221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105791603-G-A

79899221-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105791603-G-C

79899479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105792221-C-T

79899539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105792287-C-T

79899916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105792985-A-G

79899967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105793041-T-C

79899997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105793071-T-C

79900298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105793332-G-A

79900379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105793413-A-G

79900401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105793427-G-T

79900445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105793471-T-C

79900484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105793554-C-T

79900534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105793604-G-A

79900557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105793627-C-T

79900620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105793688-C-T

http://identifiers.org/hco/13/GRCh38#79900684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105793734-C-A

79900848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105793873-G-A

79900848-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105793873-G-C

79900848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105793873-G-T

79900922-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105793944-G-T

79900947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105793963-T-C

79900964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105793980-G-A

79901029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105794050-A-G

79901059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105794080-T-C

http://identifiers.org/hco/13/GRCh38#79901072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105794093-C-A

79901149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105794174-G-A

79901257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105794273-C-T

79901300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105794294-T-C

79901308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105794302-T-C

79901308-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105794302-T-G

79901381-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105794355-C-G

79901381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105794355-C-T

79901422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105794396-G-A

79901813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105794773-C-T

79901961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105794892-G-A

79902067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105794991-C-T

79902132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105795040-G-A

79902270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105795176-G-A

79902350-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105795771-A-T

79902448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105795972-G-A

79902595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105796119-G-A

http://identifiers.org/hco/13/GRCh38#79902642-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105796159-A-C

79902893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105796386-G-A

http://identifiers.org/hco/13/GRCh38#79902983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105796476-C-A

79903141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105796634-C-T

79903302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105796796-T-C

79903635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105797110-A-G

79903677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105797148-G-A

79904004-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105797444-G-C

79904013-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105797453-A-T

79904184-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105797819-T-A

79904184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105797819-T-C

79904367-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105797996-T-G

79904384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105798015-T-C

79905935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105798461-G-A

79905967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105798493-C-T

79906354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105798874-A-G

79906556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105799080-G-A

79906556-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105799080-G-C

79907021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105799424-G-A

79907361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105799678-G-A

http://identifiers.org/hco/13/GRCh38#79907811-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105800109-A-C

79908459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105800357-G-A

79908818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105800690-G-A

79908822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105800694-G-A

http://identifiers.org/hco/13/GRCh38#79908852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105800723-C-A

79908908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105800778-G-A

79908908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105800778-G-T

79908926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105800795-A-G

http://identifiers.org/hco/13/GRCh38#79908945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105800822-C-A

79908945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105800822-C-T

79908971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105800849-G-A

79908971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105800849-G-T

79909031-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105800911-G-C

79909161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105801318-G-T

79909245-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105801427-A-T

79909679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105802288-A-G

79909772-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105802380-G-C

79909807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105802412-C-T

79909998-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105802594-G-C

79910075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105802677-C-T

79910289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105802802-A-G

79910289-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105802802-A-T

79910405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105802899-G-A

http://identifiers.org/hco/13/GRCh38#79910472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105802965-C-A

79910533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105803021-G-A

79910610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105803100-G-A

79910707-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105803223-A-T

79910727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105803243-T-C

79910733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105803249-T-C

79910749-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105803265-T-A

79911103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105803615-G-T

http://identifiers.org/hco/13/GRCh38#79911460-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105803965-A-C

79911661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105804140-T-C

79911685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105804171-T-C

79911751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105804237-G-A

79912340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105806052-A-G

79912422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: non coding transcript exon variant
orthologous variants: 105806118-T-C

http://identifiers.org/hco/13/GRCh38#79912458-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105806157-A-C

http://identifiers.org/hco/13/GRCh38#79912524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105806228-C-A

79912524-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105806228-C-G

79912524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105806228-C-T

79912575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105806305-T-C

79912598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105806315-T-C

79912607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105806324-A-G

79912616-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105806332-T-A

79912744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105806458-G-T

79913062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105806807-T-C

79913099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105806845-A-G

79913180-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105806920-T-G

79913851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105807752-C-T

79913903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105807807-C-T

79914142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105808037-A-G

79914396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105808858-A-G

http://identifiers.org/hco/13/GRCh38#79914651-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105809089-C-A

79914651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105809089-C-T

http://identifiers.org/hco/13/GRCh38#79914936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105809325-C-A

79914975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105809365-G-T

79914977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105809367-T-C

79915275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105809648-T-C

79915461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105809837-G-A

79915694-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105810070-C-G

79915694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105810070-C-T

79915774-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105810154-T-G

79915804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105810183-C-T

79916526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 105810863-T-C

79916666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105811049-G-A

79916666-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105811049-G-T

79916795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105811154-G-A

79917137-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105811752-G-C

79917137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105811752-G-T

79917266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105811891-G-A

79917303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105811928-T-C

79917918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: non coding transcript exon variant
orthologous variants: 105812501-T-C

http://identifiers.org/hco/13/GRCh38#79917945-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42709
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#105812528-A-C