127941261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: 3 prime UTR variant
orthologous variants: 31856075-T-C

http://identifiers.org/hco/2/GRCh38#127941372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#31855971-C-A

127941372-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: 3 prime UTR variant
orthologous variants: 31855971-C-G

127941372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: 3 prime UTR variant
orthologous variants: 31855971-C-T

127941463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: 3 prime UTR variant
orthologous variants: 31855882-A-G

127941522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: 3 prime UTR variant
orthologous variants: 31855826-G-A

127941522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: 3 prime UTR variant
orthologous variants: 31855826-G-T

http://identifiers.org/hco/2/GRCh38#127941530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#31855818-C-A

127941530-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: 3 prime UTR variant
orthologous variants: 31855818-C-G

127941530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: 3 prime UTR variant
orthologous variants: 31855818-C-T

http://identifiers.org/hco/2/GRCh38#127941534-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#31855814-C-A

127941534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: 3 prime UTR variant
orthologous variants: 31855814-C-T

http://identifiers.org/hco/2/GRCh38#127941605-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#31855746-A-C

127941605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: 3 prime UTR variant
orthologous variants: 31855746-A-G

127941632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: 3 prime UTR variant
orthologous variants: 31855721-T-C

http://identifiers.org/hco/2/GRCh38#127941890-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#31855507-A-C

127941890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: 3 prime UTR variant
orthologous variants: 31855507-A-G

127941907-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: 3 prime UTR variant
orthologous variants: 31855490-T-A

127941907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: 3 prime UTR variant
orthologous variants: 31855490-T-C

127941907-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: 3 prime UTR variant
orthologous variants: 31855490-T-G

http://identifiers.org/hco/2/GRCh38#127941930-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#31855468-A-C

127941930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: 3 prime UTR variant
orthologous variants: 31855468-A-G

127941962-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: 3 prime UTR variant
orthologous variants: 31855424-T-A

127941962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: 3 prime UTR variant
orthologous variants: 31855424-T-C

127941962-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: 3 prime UTR variant
orthologous variants: 31855424-T-G

127942222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31855168-A-G

127942437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: missense variant
orthologous variants: 31853808-T-C

127942461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: missense variant
orthologous variants: 31853784-G-A

127942599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31853649-G-A

127942599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31853649-G-T

http://identifiers.org/hco/2/GRCh38#127942639-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#31853609-A-C

127943125-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31853447-T-A

127945425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31848527-C-T

127945588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31848362-T-C

127948825-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31846714-G-C

127948939-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31846601-G-C

127949251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31845930-A-G

127949410-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31845174-G-C

127949681-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31844916-G-C

127950010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31844634-C-T

127950045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31844598-A-G

http://identifiers.org/hco/2/GRCh38#127950052-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#31844591-A-C

127950052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31844591-A-G

127950127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31844535-G-A

127950127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31844535-G-T

127950140-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31844517-A-T

127950218-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: synonymous variant
orthologous variants: 31844439-A-T

http://identifiers.org/hco/2/GRCh38#127950318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#31844339-C-A

127950318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: missense variant
orthologous variants: 31844339-C-T

http://identifiers.org/hco/2/GRCh38#127950466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#31844202-C-A

127950578-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31844091-C-G

127955024-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: missense variant
orthologous variants: 31831893-T-A

127955234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: missense variant
orthologous variants: 31831683-G-A

127955375-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31831541-A-T

127976071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31825425-C-T

127976135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31825365-T-C

127976141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31825359-C-T

127976200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31825293-A-G

127976601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31824899-A-G

127978306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31821949-C-T

127978385-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31821875-G-C

127978560-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31821692-T-G

127978796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31821499-G-A

127978796-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31821499-G-C

127978841-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31821455-A-T

127986724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31815270-T-C

127986857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: missense variant
orthologous variants: 31815163-G-A

127986885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: missense variant
orthologous variants: 31815135-T-C

127986976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31815041-G-A

127986976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31815041-G-T

http://identifiers.org/hco/2/GRCh38#127989428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#31813963-C-A

127989428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31813963-C-T

127989581-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: missense variant
orthologous variants: 31813705-G-C

127989594-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: missense variant
orthologous variants: 31813692-G-C

127989594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: missense variant
orthologous variants: 31813692-G-T

127989596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: missense variant
orthologous variants: 31813690-G-A

127989597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: missense variant
orthologous variants: 31813689-T-C

127989627-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: missense variant
orthologous variants: 31813659-T-G

127989631-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: missense variant
orthologous variants: 31813655-G-C

127989638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: missense variant
orthologous variants: 31813648-G-A

127989922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31813386-A-G

127990089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31813197-C-T

127990098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31813188-T-C

127990180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31812985-G-A

http://identifiers.org/hco/2/GRCh38#127990210-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#31812954-A-C

127992847-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31810844-A-T

127992947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31810751-A-G

127993054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31810653-C-T

127993195-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: missense variant
orthologous variants: 31810520-T-G

http://identifiers.org/hco/2/GRCh38#127993344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#31810372-C-A

127993344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31810372-C-T

127993456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31810278-G-A

127993456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31810278-G-T

127993494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31810248-G-A

127993593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31810121-C-T

127994015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31809616-C-T

127994091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31809548-T-C

127994370-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31809353-T-A

127994961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31808930-T-C

http://identifiers.org/hco/2/GRCh38#127995383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#31808612-C-A

127995417-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31808585-T-A

127995664-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31808353-G-C

127995729-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31808224-C-G

127995883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31807956-T-C

127995958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31807880-C-T

127995976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31807862-G-T

http://identifiers.org/hco/2/GRCh38#127996313-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#31807580-C-A

127996313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31807580-C-T

http://identifiers.org/hco/2/GRCh38#127996314-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#31807579-A-C

127996314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31807579-A-G

127996327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31807570-A-G

127996331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31807566-C-T

http://identifiers.org/hco/2/GRCh38#127996508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#31807388-C-A

127996508-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31807388-C-G

127996508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31807388-C-T

http://identifiers.org/hco/2/GRCh38#127999664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#31800136-C-A

127999664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31800136-C-T

http://identifiers.org/hco/2/GRCh38#127999675-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#31800123-A-C

127999675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31800123-A-G

127999687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31800111-G-A

127999687-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31800111-G-T

127999690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31800108-G-A

127999690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31800108-G-T

127999830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: missense variant
orthologous variants: 31799971-G-A

127999830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: missense variant
orthologous variants: 31799971-G-T

127999835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: synonymous variant
orthologous variants: 31799966-T-C

127999887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31799913-T-C

http://identifiers.org/hco/2/GRCh38#127999893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#31799907-C-A

128000022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31799810-C-T

128000079-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: missense variant
orthologous variants: 31799754-G-C

128000079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: missense variant
orthologous variants: 31799754-G-T

128000225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31799606-A-G

128000350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: missense variant
orthologous variants: 31799496-G-A

128000377-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: missense variant
orthologous variants: 31799469-G-C

128000473-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31799347-C-G

128000584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31799250-T-C

128000596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31799238-G-A

128000596-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31799238-G-C

128000596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31799238-G-T

128000718-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31799095-C-G

128000779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31799005-G-T

128000897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31798817-C-T

128004728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31793920-G-A

http://identifiers.org/hco/2/GRCh38#128005074-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#31793532-A-C

128005301-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31793284-G-T

128005636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31793003-T-C

128005636-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31793003-T-G

http://identifiers.org/hco/2/GRCh38#128005670-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#31792974-A-C

128005839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31792927-A-G

http://identifiers.org/hco/2/GRCh38#128006146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#31792532-C-A

128006368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31792189-T-C

128006462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31792107-T-C

128006806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31792073-G-T

128006829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31792050-A-G

128007019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31791847-G-A

128007030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31791833-A-G

128007882-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31790371-T-A

128010284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: missense variant
orthologous variants: 31786662-G-A

128010293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: missense variant
orthologous variants: 31786653-G-A

128010302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: missense variant
orthologous variants: 31786644-G-A

128010327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: missense variant
orthologous variants: 31786619-T-C

128010371-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: missense variant
orthologous variants: 31786575-G-C

http://identifiers.org/hco/2/GRCh38#128010453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#31786483-C-A

128010453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31786483-C-T

128010484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31786452-G-A

128012972-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31783737-G-C

128012972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31783737-G-T

128012997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31783712-G-A

128013112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: missense variant
orthologous variants: 31783584-G-A

128013181-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31783515-T-A

128013181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31783515-T-C

128013216-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31783484-T-A

128013216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31783484-T-C

128013264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31783419-G-A

128013264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31783419-G-T

128013307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31783376-G-A

128014769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31782732-T-C

128014796-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 31782714-T-G

128014847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: missense variant
orthologous variants: 31782663-G-A

128014949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31782561-G-A

128014953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31782557-G-A

128014953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31782557-G-T

http://identifiers.org/hco/2/GRCh38#128015035-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#31782417-A-C

128015035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31782417-A-G

http://identifiers.org/hco/2/GRCh38#128015051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#31782355-C-A

128015051-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31782355-C-G

http://identifiers.org/hco/2/GRCh38#128015060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#31782329-C-A

128015386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31781965-A-G

128016210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31781462-G-A

128016326-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31781402-T-A

128016411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: missense variant
orthologous variants: 31781321-A-G

128016648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31781090-G-A

128016648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31781090-G-T

128016669-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31781069-T-A

128016669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31781069-T-C

128016685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31781056-T-C

128017004-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31780760-T-A

128017025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31780750-T-C

http://identifiers.org/hco/2/GRCh38#128017194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#31780683-C-A

128017194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31780683-C-T

128017483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31780514-T-C

http://identifiers.org/hco/2/GRCh38#128017555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#31780452-C-A

128017555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31780452-C-T

http://identifiers.org/hco/2/GRCh38#128017573-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#31780424-A-C

128017672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 31780335-T-C

128017843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: missense variant
orthologous variants: 31780164-G-A

http://identifiers.org/hco/2/GRCh38#128017867-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#31780140-A-C

http://identifiers.org/hco/2/GRCh38#128018030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#31779989-C-A

128018030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31779989-C-T

128018033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31779986-G-A

128018033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31779986-G-T

128018247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31779061-A-G

128020142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31775795-T-C

128020164-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31775773-T-G

128020215-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31775722-G-C

128020606-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31775435-T-A

128020606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31775435-T-C

128021020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31775041-T-C

128021513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31774422-T-C

128021574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31774276-T-C

128021591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31774253-C-T

128021655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31774172-C-T

128021684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31774147-G-A

128021701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31774135-C-T

128021850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31773966-C-T

128021851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31773965-A-G

128022213-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31773294-G-C

128022264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31773245-A-G

128022418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31773098-C-T

128022420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31773096-T-C

http://identifiers.org/hco/2/GRCh38#128025032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#31770043-C-A

128025225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31769888-T-C

http://identifiers.org/hco/2/GRCh38#128025840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#31769473-C-A

128026018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31769293-G-A

128026163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31769169-G-A

128026163-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31769169-G-C

128026163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31769169-G-T

128026350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31768984-A-G

128026624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31768726-T-C

128027079-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron_variant, undefined
orthologous variants: 31768303-T-A

128027079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron_variant, undefined
orthologous variants: 31768303-T-C

128027079-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron_variant, undefined
orthologous variants: 31768303-T-G

128027094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 31768288-G-A

128027094-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron_variant, missense_variant, splice_region_variant, undefined
orthologous variants: 31768288-G-C

128027094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron_variant, missense_variant, splice_region_variant, undefined
orthologous variants: 31768288-G-T

128027210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 31768233-G-A

128027210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 31768233-G-T

http://identifiers.org/hco/2/GRCh38#128027215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#31768228-C-A

128027215-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 31768228-C-G

128027215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 31768228-C-T

128027221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 31768222-G-A

128027221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 31768222-G-T

http://identifiers.org/hco/2/GRCh38#128027293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#31768149-C-A

128027293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 31768149-C-T

128027334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31768108-G-A

128027334-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31768108-G-C

http://identifiers.org/hco/2/GRCh38#128027393-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#31768051-A-C

128027393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron_variant, undefined
orthologous variants: 31768051-A-G

128027393-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron_variant, undefined
orthologous variants: 31768051-A-T

128027620-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: intron variant
orthologous variants: 31767817-C-G

http://identifiers.org/hco/2/GRCh38#128028042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#31767451-C-A

http://identifiers.org/hco/2/GRCh38#128028065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#31767428-C-A

128028065-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: 5 prime UTR variant
orthologous variants: 31767428-C-G

128028065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29813
most severe consequence: 5 prime UTR variant
orthologous variants: 31767428-C-T