226548780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 5 prime UTR variant
orthologous variants: 180311010-A-G

226548780-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 5 prime UTR variant
orthologous variants: 180311010-A-T

226548811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 5 prime UTR variant
orthologous variants: 180310972-G-A

226548811-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 5 prime UTR variant
orthologous variants: 180310972-G-C

226549037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: missense variant
orthologous variants: 180310760-G-A

226549037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: missense variant
orthologous variants: 180310760-G-T

226549209-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180310558-T-A

226549209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180310558-T-C

226549209-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180310558-T-G

226549474-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180310305-C-G

226549640-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180310133-C-G

226549682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180310098-C-T

226549815-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180309970-C-G

226549930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180309881-G-A

226550385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180309441-T-C

226550695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron_variant, undefined
orthologous variants: 180309157-G-A

226550748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron_variant, undefined
orthologous variants: 180309098-C-T

226550916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180308948-A-G

http://identifiers.org/hco/1/GRCh38#226551067-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#180308808-A-C

226551541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180308175-A-G

226552383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180306927-C-T

226552579-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180306717-G-C

226552584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180306712-G-A

226552804-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180306486-G-C

226553272-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180305123-T-G

226553295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180305100-T-C

226553401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180304843-C-T

226553411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180304833-G-A

226553700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180304525-G-A

226553723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180304501-G-A

http://identifiers.org/hco/1/GRCh38#226553791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#180304434-C-A

226553866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180304363-C-T

226553889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180304340-A-G

226554017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180304203-C-T

226554052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180304165-A-G

226554101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180304117-G-A

226554336-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180303957-A-T

http://identifiers.org/hco/1/GRCh38#226554343-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#180303951-A-C

226554358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180303935-A-G

226554442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180303854-A-G

226554478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180303818-A-G

http://identifiers.org/hco/1/GRCh38#226554625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#180303682-C-A

226554641-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180303666-A-T

226554715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180303605-G-A

226554995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180303343-T-C

226555116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180303245-G-A

226555116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180303245-G-T

226555302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180303085-C-T

226558384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180300725-C-T

226558524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180300240-C-T

226558607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180300172-G-A

226558607-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180300172-G-C

226558784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180299996-G-A

226558836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180299948-G-A

226559046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180299783-T-C

226559304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180299506-C-T

226559349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180299462-G-A

226559349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180299462-G-T

http://identifiers.org/hco/1/GRCh38#226559379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#180299436-C-A

226559379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180299436-C-T

226560853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180298933-C-T

226560885-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180298901-C-G

226561135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180298742-C-T

226561183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180298684-C-T

226561275-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180298600-G-C

226561523-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180298000-G-C

226562136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180297472-G-T

226562379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180297191-G-A

226562379-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180297191-G-C

226563009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180296664-A-G

226563418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180296124-C-T

http://identifiers.org/hco/1/GRCh38#226563499-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#180296053-A-C

226563499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180296053-A-G

226563508-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180296047-T-A

http://identifiers.org/hco/1/GRCh38#226564046-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#180295550-A-C

226564152-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180295444-T-G

226564551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180295180-T-C

226564684-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180295053-C-G

http://identifiers.org/hco/1/GRCh38#226564909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#180294291-C-A

226565119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180294112-G-A

226565119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180294112-G-T

226565407-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180293590-G-C

226565413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180293584-G-A

226565413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180293584-G-T

226565469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180293516-C-T

226565906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180293119-A-G

226566602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180292458-G-T

226566636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180292425-C-T

226567219-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180291892-G-C

226567795-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180290879-T-A

226567795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180290879-T-C

226568012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180290692-T-C

226568162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180290544-G-A

226568354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180290286-G-T

226568435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180290205-G-A

226568518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180290122-C-T

http://identifiers.org/hco/1/GRCh38#226568955-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#180289783-A-C

http://identifiers.org/hco/1/GRCh38#226569145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#180289550-C-A

226569397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180289197-C-T

226569698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180288950-A-G

226569998-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180288652-T-A

226570007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180288645-C-T

226570399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180288329-G-A

226572068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180287305-G-A

226572290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180287107-G-A

226572300-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180287097-A-T

226576102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180285868-A-G

226576305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180285709-G-T

226576747-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180284298-C-G

226576771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180284274-G-A

226576921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180284169-A-G

226576924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180284166-G-A

226576938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180284152-A-G

226577320-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180283813-T-A

226577320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180283813-T-C

http://identifiers.org/hco/1/GRCh38#226577410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#180283757-C-A

226577503-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180283657-A-T

226577582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180283567-C-T

226579095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180281948-G-T

226579138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180281905-C-T

226579239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180281822-T-C

226584683-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180278511-T-A

226584698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180278496-G-A

226584827-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180278370-T-A

226584921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180278248-A-G

226585564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180277706-G-A

226585576-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180277694-T-G

226585696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180277614-C-T

226585936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180277374-T-C

http://identifiers.org/hco/1/GRCh38#226586583-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#180276634-A-C

226586780-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180276450-G-C

226586864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180276366-C-T

226586939-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180276309-C-G

226586939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180276309-C-T

226586993-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180276262-C-G

226586993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180276262-C-T

226587085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180276170-T-C

226587092-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180276163-G-C

226587138-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180276128-T-G

226587310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180275959-G-A

226587331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180275934-T-C

226588217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180275581-T-C

226588276-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180275514-C-G

226588276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180275514-C-T

226589028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180274884-A-G

226589731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron_variant, undefined
orthologous variants: 180274180-T-C

226589834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180274126-A-G

226591855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180273463-G-A

226592539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180273002-A-G

226592683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180272869-T-C

226593375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180272554-C-T

226593464-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180272468-A-T

226593620-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180272317-C-G

226594113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180271889-C-T

226594230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180271808-A-G

226596642-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180270415-T-A

226596642-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180270415-T-G

226596651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180270406-G-A

226596651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180270406-G-T

http://identifiers.org/hco/1/GRCh38#226596683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#180270380-C-A

226596683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180270380-C-T

226596684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180270379-G-A

226596684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180270379-G-T

http://identifiers.org/hco/1/GRCh38#226596750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#180270338-C-A

226596750-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180270338-C-G

226596750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180270338-C-T

226596870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: missense variant
orthologous variants: 180270218-T-C

226596972-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: missense variant
orthologous variants: 180270116-A-T

http://identifiers.org/hco/1/GRCh38#226597111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#180269873-C-A

226597111-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180269873-C-G

226597111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180269873-C-T

http://identifiers.org/hco/1/GRCh38#226597327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#180269488-C-A

226597335-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180269480-T-A

http://identifiers.org/hco/1/GRCh38#226597382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#180269440-C-A

http://identifiers.org/hco/1/GRCh38#226597491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#180269354-C-A

226597548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180269307-G-T

226597607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180269259-G-A

226597857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180269004-G-T

226597910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180268963-G-A

226597991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180268935-C-T

226598023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180268914-G-A

226598048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180268890-T-C

226598169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180268799-G-A

226598169-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180268799-G-C

226598797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180267788-T-C

http://identifiers.org/hco/1/GRCh38#226598799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#180267786-C-A

226598813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180267775-G-A

http://identifiers.org/hco/1/GRCh38#226598831-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#180267757-A-C

226599327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180267654-T-C

226599371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180267610-C-T

226599419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180267568-G-T

http://identifiers.org/hco/1/GRCh38#226599565-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#180267463-A-C

226599565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180267463-A-G

226599608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180267424-A-G

226599803-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron_variant, undefined
orthologous variants: 180267260-C-G

226600220-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180266968-G-C

http://identifiers.org/hco/1/GRCh38#226600453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#180266853-C-A

226600453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180266853-C-T

226600539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180266766-A-G

http://identifiers.org/hco/1/GRCh38#226600543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#180266762-C-A

226600543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron variant
orthologous variants: 180266762-C-T

226600632-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 180266710-T-A

226600807-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180266593-A-T

http://identifiers.org/hco/1/GRCh38#226600843-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#180266568-A-C

226602087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 180265848-G-A

226602087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 180265848-G-T

226602258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: 180265679-G-A

226602388-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: 180265572-G-C

226602434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: 180265526-G-A

226602434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: 180265526-G-T

226602448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: 180265512-G-A

226602448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: 180265512-G-T

http://identifiers.org/hco/1/GRCh38#226602467-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#180265493-A-C

http://identifiers.org/hco/1/GRCh38#226602505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#180265454-C-A

226602505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: 180265454-C-T

226602573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: 180265379-A-G

226602573-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: 180265379-A-T

226602695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: 180265324-G-A

226602695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: 180265324-G-T

226602698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: 180265321-T-C

226602699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: 180265320-G-A

226602699-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: 180265320-G-T

http://identifiers.org/hco/1/GRCh38#226602874-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#180265135-C-A

http://identifiers.org/hco/1/GRCh38#226603003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#180265011-C-A

http://identifiers.org/hco/1/GRCh38#226603025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#180264989-C-A

226603201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: 180264835-G-T

http://identifiers.org/hco/1/GRCh38#226603222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#180264813-C-A

226603429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: 180264662-T-C

226603462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: 180264629-A-G

226603518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: 180264574-C-T

226603562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: 180264544-G-T

http://identifiers.org/hco/1/GRCh38#226603651-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#180264421-C-A

http://identifiers.org/hco/1/GRCh38#226603667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#180264403-C-A

226603747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: 180264278-G-A

226603747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: 180264278-G-T

http://identifiers.org/hco/1/GRCh38#226603758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#180264267-C-A

226603758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: 180264267-C-T

226603767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: 180264258-G-A

226603767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: 180264258-G-T

226603774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: 180264251-T-C

226603774-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: 180264251-T-G

226603796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: 180264229-G-A

226603861-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: 180264184-C-G

226603969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: 180264129-C-T

226603971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: 180264127-G-A

226603983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: 180264115-G-A

226603983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: 180264115-G-T

226603985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: 180264113-T-C

226603989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: 180264109-T-C

226604181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: 180263959-T-C

226604257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: 180263883-G-T

http://identifiers.org/hco/1/GRCh38#226604361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#180263786-C-A

226604361-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: 180263786-C-G

http://identifiers.org/hco/1/GRCh38#226604661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#180263575-C-A

226604828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: 180263446-A-G

226604830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: 180263444-A-G

226604938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: 180263336-T-C

226605543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: 180263883-T-C

226605544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: 180263884-G-A

226605619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: 180263959-C-T

226605710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: 180264056-C-T

226606004-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: 180262297-G-C

http://identifiers.org/hco/1/GRCh38#226606048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#180262254-C-A

226606190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: 180262123-G-A

226606190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: 180262123-G-T

226606714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: 180261989-A-G

226606754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: 180261951-C-T

226606769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: 180261940-G-A

226606790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: 180261922-A-G

226606848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: 180261870-A-G

http://identifiers.org/hco/1/GRCh38#226606857-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#180261861-A-C

226606857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: 180261861-A-G

http://identifiers.org/hco/1/GRCh38#226606887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#180261825-C-A

226606889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: 180261823-A-G

226606960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: 180261752-C-T

226607069-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: 180261657-G-C

226607069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: 180261657-G-T

226607196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: 180261578-T-C

226607285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: 180261507-T-C

226607478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: 180261361-A-G

226607520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: 180261320-G-A

226607520-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: 180261320-G-C

226607520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: 180261320-G-T

226608745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: 180260415-A-G

226608748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: 180260412-C-T

http://identifiers.org/hco/1/GRCh38#226608936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#180260251-C-A

226608936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: 180260251-C-T

226609007-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 180260177-A-T

226609047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30491
most severe consequence: 3 prime UTR variant
orthologous variants: 180260141-T-C