http://identifiers.org/hco/4/GRCh38#46035940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#70906519-C-A

46036049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: 3 prime UTR variant
orthologous variants: 70906627-C-T

http://identifiers.org/hco/4/GRCh38#46036163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#70906724-C-A

46036265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: 3 prime UTR variant
orthologous variants: 70906822-T-C

46036266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: 3 prime UTR variant
orthologous variants: 70906823-C-T

46036315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: 3 prime UTR variant
orthologous variants: 70906876-T-C

46038306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: 3 prime UTR variant
orthologous variants: 70908660-T-C

46038317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: 3 prime UTR variant
orthologous variants: 70908678-T-C

46038345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: 3 prime UTR variant
orthologous variants: 70908703-A-G

46038386-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: 3 prime UTR variant
orthologous variants: 70908744-C-G

46038397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: 3 prime UTR variant
orthologous variants: 70908755-A-G

46038402-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: 3 prime UTR variant
orthologous variants: 70908760-C-G

46038468-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: 3 prime UTR variant
orthologous variants: 70908826-T-A

46038508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: 3 prime UTR variant
orthologous variants: 70908853-A-G

46038557-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: 3 prime UTR variant
orthologous variants: 70908902-T-A

46038579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: 3 prime UTR variant
orthologous variants: 70908915-G-A

46038579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: 3 prime UTR variant
orthologous variants: 70908915-G-T

46038615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: 3 prime UTR variant
orthologous variants: 70908954-G-A

46038615-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: 3 prime UTR variant
orthologous variants: 70908954-G-C

46038879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: 3 prime UTR variant
orthologous variants: 70909224-T-C

46039108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: 3 prime UTR variant
orthologous variants: 70909405-A-G

46039142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: 3 prime UTR variant
orthologous variants: 70909439-C-T

46039977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: 3 prime UTR variant
orthologous variants: 70910305-T-C

46040005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: 3 prime UTR variant
orthologous variants: 70910331-T-C

46040183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: 3 prime UTR variant
orthologous variants: 70910487-T-C

46040192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: 3 prime UTR variant
orthologous variants: 70910496-T-C

http://identifiers.org/hco/4/GRCh38#46040341-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#70910641-C-A

46040341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: 3 prime UTR variant
orthologous variants: 70910641-C-T

46040349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: 3 prime UTR variant
orthologous variants: 70910649-G-A

http://identifiers.org/hco/4/GRCh38#46040454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#70910844-C-A

http://identifiers.org/hco/4/GRCh38#46040540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#70910923-C-A

http://identifiers.org/hco/4/GRCh38#46040618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#70910997-C-A

46040899-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: 3 prime UTR variant
orthologous variants: 70911276-T-G

http://identifiers.org/hco/4/GRCh38#46041283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#70911659-C-A

46041283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70911659-C-T

46041349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70911726-G-A

46041349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70911726-G-T

46041378-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70911776-T-A

46041378-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70911776-T-G

http://identifiers.org/hco/4/GRCh38#46041379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#70911777-C-A

46041440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70911842-A-G

46041466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70911872-C-T

http://identifiers.org/hco/4/GRCh38#46041566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#70911974-C-A

46041566-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70911974-C-G

46041750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70912144-A-G

46041758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70912152-G-A

46041758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70912152-G-T

46041969-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70912337-A-T

46045873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70914502-T-C

46046360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70914911-C-T

46047156-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70916157-A-T

46047269-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70916266-G-C

46047269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70916266-G-T

46047338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70916336-A-G

46047576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70916607-C-T

46047596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70916626-A-G

46047788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70916765-T-C

46047860-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70916836-T-G

46049143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70917723-C-T

46049151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70917731-G-A

46049204-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70917781-T-G

46049247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70917847-T-C

http://identifiers.org/hco/4/GRCh38#46049887-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#70918676-A-C

46049887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70918676-A-G

46049938-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70918727-G-C

46050309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70926610-C-T

46050473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70926779-C-T

46050658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70926970-A-G

46050741-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70927052-T-A

46050741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70927052-T-C

46050810-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70927117-T-A

46051044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70927344-C-T

46051568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: synonymous variant
orthologous variants: 70931755-A-G

46051598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: synonymous variant
orthologous variants: 70931785-A-G

46051598-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: synonymous variant
orthologous variants: 70931785-A-T

http://identifiers.org/hco/4/GRCh38#46051655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#70931842-C-A

46051655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70931842-C-T

46051676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70931868-A-G

46051827-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70932008-T-A

46051935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70932118-G-A

46052046-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70932204-T-A

46052046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70932204-T-C

46052107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70932251-A-G

46052516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70932661-C-T

46052631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70932969-A-G

46052728-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70933114-A-T

46052825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70933208-A-G

46052826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70933209-T-C

46052894-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70933276-A-T

46057092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70933474-G-T

http://identifiers.org/hco/4/GRCh38#46057152-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#70933544-A-C

46057201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70933597-T-C

46057331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70933693-C-T

46057481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70933820-C-T

46057608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70933936-T-C

46057728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70934016-G-T

http://identifiers.org/hco/4/GRCh38#46057835-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#70934098-A-C

http://identifiers.org/hco/4/GRCh38#46057858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#70934121-C-A

46057858-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70934121-C-G

46058063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70934324-C-T

46058079-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70934339-G-C

46058079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70934339-G-T

46058080-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70934340-T-G

46058112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70934373-G-T

46058120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70934381-G-A

46058120-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70934381-G-C

46058120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70934381-G-T

46058302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: synonymous variant
orthologous variants: 70934546-G-A

46058302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: synonymous variant
orthologous variants: 70934546-G-T

46058429-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70934685-A-T

46058603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: synonymous variant
orthologous variants: 70935523-T-C

46058663-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70935593-G-C

46058663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70935593-G-T

http://identifiers.org/hco/4/GRCh38#46058667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#70935597-C-A

46058667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70935597-C-T

http://identifiers.org/hco/4/GRCh38#46058717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#70935648-C-A

http://identifiers.org/hco/4/GRCh38#46058742-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#70935673-A-C

46058742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70935673-A-G

46060370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70935978-C-T

46061027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70936560-T-C

46061169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70936703-A-G

46061169-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70936703-A-T

46061278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70936796-G-A

46061361-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70936867-T-A

46061396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70936903-C-T

46061589-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70937088-G-C

46064149-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70937483-C-G

http://identifiers.org/hco/4/GRCh38#46064376-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#70937932-C-A

46064376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70937932-C-T

46064552-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70938102-T-A

46064552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70938102-T-C

46064552-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70938102-T-G

46064567-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70938117-T-A

46064567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70938117-T-C

46064581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70938129-T-C

46064604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70938149-G-A

46064604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70938149-G-T

46064613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70938158-A-G

46064642-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70938187-T-A

46064657-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70938202-A-T

http://identifiers.org/hco/4/GRCh38#46064673-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#70938208-A-C

46064673-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70938208-A-T

46064751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70938294-A-G

46064782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70938321-A-G

46065122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70939391-C-T

46065155-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70939424-T-G

46065286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70939539-A-G

46065286-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70939539-A-T

46065346-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70939574-T-G

46065633-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70939857-T-A

46065633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70939857-T-C

46065652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70939875-G-A

46065652-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70939875-G-C

46065652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70939875-G-T

46065666-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70939889-T-A

46065666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70939889-T-C

46066092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70940726-G-A

46066195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70940787-A-G

http://identifiers.org/hco/4/GRCh38#46066262-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#70940857-A-C

46066287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70940882-A-G

46066517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70941093-C-T

46066990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70941439-T-C

46067162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70941616-C-T

46067403-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70941811-T-G

46067606-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70941993-T-G

46067632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70942012-A-G

46068412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70942735-C-T

46068472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70942847-G-A

46068486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70942861-G-T

46068492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70942867-T-C

46068878-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70943273-T-A

46068878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70943273-T-C

46069012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70943397-A-G

46069287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70943660-T-C

46069396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70943732-C-T

46069507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70943833-A-G

http://identifiers.org/hco/4/GRCh38#46069703-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#70943976-A-C

46069703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70943976-A-G

46070098-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70944356-T-A

http://identifiers.org/hco/4/GRCh38#46070387-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#70944618-A-C

46070793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70944932-A-G

http://identifiers.org/hco/4/GRCh38#46072456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#70945212-C-A

46072681-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70945427-T-A

46078300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70947023-T-C

46079074-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70947489-T-G

46079078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70947493-T-C

46079078-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70947493-T-G

46079248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 70947625-C-T

46079254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 70947631-G-A

46079778-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70948628-G-C

46080331-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70949272-C-G

46081339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70949625-C-T

46081456-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70949742-A-T

46081489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70949775-T-C

46081597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron_variant, undefined
orthologous variants: 70950203-A-G

46083931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70951950-A-G

46084062-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70952065-T-A

46084062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70952065-T-C

http://identifiers.org/hco/4/GRCh38#46084107-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#70952102-A-C

46084183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70952167-G-T

46084251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70952229-A-G

http://identifiers.org/hco/4/GRCh38#46084572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#70954008-C-A

46084572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70954008-C-T

46084724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70954162-A-G

46084816-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70954254-T-A

46084816-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70954254-T-G

46084853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70954287-T-C

46085100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70954511-G-T

46085221-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70954620-T-A

46085244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70954640-G-T

46085285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70954681-C-T

46085648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70955185-C-T

46085720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70955268-A-G

46086452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70955968-A-G

46086833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70956363-T-C

46087043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70956482-T-C

http://identifiers.org/hco/4/GRCh38#46087201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#70956619-C-A

46087234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70956651-A-G

46087274-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70956687-T-A

http://identifiers.org/hco/4/GRCh38#46097145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#70973257-C-A

http://identifiers.org/hco/4/GRCh38#46097366-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#70973465-A-C

46097398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70973500-A-G

46097429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70973522-A-G

46097430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70973523-T-C

46097430-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70973523-T-G

http://identifiers.org/hco/4/GRCh38#46097499-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#70973589-A-C

46097499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70973589-A-G

46097593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70973663-A-G

46097678-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70973742-G-C

46097823-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70973879-T-A

46100942-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70979482-T-A

46101002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70979541-A-G

46101082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70979611-G-T

46101325-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70980066-T-A

46101325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70980066-T-C

46101329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70980070-G-A

46101338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70980079-A-G

46101344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70980085-G-A

46101369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70980124-C-T

46101395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70980147-G-A

46101395-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70980147-G-C

46101711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70980495-T-C

http://identifiers.org/hco/4/GRCh38#46101779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#70980567-C-A

46101820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70980681-A-G

http://identifiers.org/hco/4/GRCh38#46101964-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#70980841-A-C

46102318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70981197-A-G

46102411-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70981237-C-G

46102411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70981237-C-T

http://identifiers.org/hco/4/GRCh38#46102480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#70981306-C-A

46102480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70981306-C-T

46102502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70981326-T-C

46102892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70981696-A-G

46102927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70981731-T-C

46103248-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70982043-G-C

http://identifiers.org/hco/4/GRCh38#46103258-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#70982053-A-C

46103686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70982505-A-G

46103710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70982526-T-C

46103869-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70982677-T-A

46103869-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70982677-T-G

46103896-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70982712-T-G

46103957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70982748-T-C

http://identifiers.org/hco/4/GRCh38#46104075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#70982804-C-A

46104075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70982804-C-T

46104134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70982855-A-G

46104624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70983294-A-G

46104628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70983298-C-T

46104739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70983398-T-C

http://identifiers.org/hco/4/GRCh38#46104807-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#70983461-A-C

46104811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70983464-G-A

46108151-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70985723-T-A

46108646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70986291-G-A

46108677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70986317-C-T

46108709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70986357-G-A

46108861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70986515-T-C

46108922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70986554-T-C

46108930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70986559-A-G

46113594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70986983-T-C

46113624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70987009-G-A

46113697-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70987091-G-C

46113815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70987162-T-C

46113820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70987169-G-A

46113856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70987205-A-G

46115910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70991735-A-G

46115980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70991799-C-T

46116156-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70992175-C-G

46116219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70992239-T-C

46116342-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70992361-T-A

46116350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70992367-A-G

46116619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70992628-G-T

http://identifiers.org/hco/4/GRCh38#46116634-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#70992641-A-C

46116646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70992653-T-C

http://identifiers.org/hco/4/GRCh38#46116828-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#70992808-A-C

46117083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70992869-T-C

46117254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70993042-A-G

46117352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70993130-G-A

46117414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70993195-G-A

46117414-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70993195-G-C

46117458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70993237-G-T

46118437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70993442-C-T

46118653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70993641-C-T

46118935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70993905-C-T

46119013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70993981-T-C

46119014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70993982-A-G

46119115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70994064-G-A

46119354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70994333-T-C

46119465-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70994434-T-A

46119465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70994434-T-C

46119518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70994476-C-T

46119519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70994477-T-C

http://identifiers.org/hco/4/GRCh38#46119778-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#70996057-A-C

46120198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70996407-A-G

46120252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70996470-T-C

46120273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70996491-C-T

46120385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70996621-A-G

46120420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70996653-T-C

46120526-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70996762-T-G

46120556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70996791-C-T

46121001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70997197-A-G

46121176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70997375-C-T

http://identifiers.org/hco/4/GRCh38#46121236-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#70997433-A-C

46121805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70997693-C-T

46121903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70997800-G-A

http://identifiers.org/hco/4/GRCh38#46121955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#70997847-C-A

http://identifiers.org/hco/4/GRCh38#46121987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#70997879-C-A

46122064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70997959-G-T

46122393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70998280-T-C

46122789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70998599-T-C

46122854-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70998664-T-A

46122950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70998756-G-A

46122978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70998776-T-C

46123355-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70999050-C-G

46123355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70999050-C-T

46123479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70999175-G-T

http://identifiers.org/hco/4/GRCh38#46123717-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#70999392-A-C

46123717-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70999392-A-T

46123744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: intron variant
orthologous variants: 70999414-A-G

46123915-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: 5 prime UTR variant
orthologous variants: 70999564-G-C

http://identifiers.org/hco/4/GRCh38#46124049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#70999692-C-A

46124049-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: 5 prime UTR variant
orthologous variants: 70999692-C-G

46124049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4086
most severe consequence: 5 prime UTR variant
orthologous variants: 70999692-C-T