135045468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40445768-G-T

135045494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40445794-G-A

135045494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40445794-G-T

135045537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40445812-G-A

135045537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40445812-G-T

135045541-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40445816-T-A

135045541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40445816-T-C

http://identifiers.org/hco/4/GRCh38#135045565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40445840-C-A

135045565-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40445840-C-G

135045565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40445840-C-T

135045571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40445846-A-G

135045572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40445847-A-G

135045572-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40445847-A-T

135045574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40445849-A-G

135045574-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40445849-A-T

135045581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40445856-G-A

135045581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40445856-G-T

135045589-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40445864-T-A

135045589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40445864-T-C

135045616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40445891-G-A

135045616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40445891-G-T

135045631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40445906-T-C

http://identifiers.org/hco/4/GRCh38#135045633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40445908-C-A

135045633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40445908-C-T

135045635-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40445910-T-A

135045635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40445910-T-C

135045635-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40445910-T-G

135045643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40445918-G-A

135045643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40445918-G-T

135045646-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40445921-T-A

135045646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40445921-T-C

135045646-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40445921-T-G

135045656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40445931-G-A

135045656-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40445931-G-C

135045656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40445931-G-T

135045663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40445938-G-A

135045663-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40445938-G-C

135045663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40445938-G-T

http://identifiers.org/hco/4/GRCh38#135045667-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40445942-A-C

135045667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40445942-A-G

http://identifiers.org/hco/4/GRCh38#135045668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40445943-C-A

135045668-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40445943-C-G

135045668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40445943-C-T

http://identifiers.org/hco/4/GRCh38#135045679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40445954-C-A

135045679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40445954-C-T

http://identifiers.org/hco/4/GRCh38#135045681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40445956-C-A

135045681-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40445956-C-G

135045681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40445956-C-T

135045692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40445967-T-C

135045703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40445978-T-C

135045715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40445990-G-A

135045715-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40445990-G-T

http://identifiers.org/hco/4/GRCh38#135045721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40445996-C-A

135045721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40445996-C-T

135045728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446003-A-G

http://identifiers.org/hco/4/GRCh38#135045739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446014-C-A

135045739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446014-C-T

135045747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446022-A-G

http://identifiers.org/hco/4/GRCh38#135045748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446023-C-A

135045748-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446023-C-G

135045752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446027-G-A

135045752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446027-G-T

http://identifiers.org/hco/4/GRCh38#135045757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446032-C-A

135045758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446033-A-G

http://identifiers.org/hco/4/GRCh38#135045760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446035-C-A

135045760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446035-C-T

135045768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446043-T-C

135045768-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446043-T-G

135045778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446053-G-A

135045778-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446053-G-C

135045778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446053-G-T

135045784-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446059-T-A

http://identifiers.org/hco/4/GRCh38#135045785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446060-C-A

135045785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446060-C-T

http://identifiers.org/hco/4/GRCh38#135045786-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446061-A-C

135045786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446061-A-G

135045788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446063-G-A

135045788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446063-G-T

http://identifiers.org/hco/4/GRCh38#135045802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446077-C-A

135045802-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446077-C-G

135045802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446077-C-T

135045805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446080-G-A

135045805-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446080-G-C

135045805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446080-G-T

135045809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446084-G-A

135045809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446084-G-T

135045811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446086-T-C

135045827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446102-G-A

135045827-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446102-G-C

135045827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446102-G-T

135045833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446108-G-A

135045833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446108-G-T

http://identifiers.org/hco/4/GRCh38#135045847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446122-C-A

135045847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446122-C-T

135045853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446128-T-C

135045854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446129-G-A

135045854-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446129-G-C

135045854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446129-G-T

135045855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446130-G-A

135045855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446130-G-T

135045864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446139-G-A

135045864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446139-G-T

135045865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446140-A-G

135045865-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446140-A-T

135045866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446141-G-T

http://identifiers.org/hco/4/GRCh38#135045890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446165-C-A

135045903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446179-A-G

135045911-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446187-T-A

135045912-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446188-T-G

135045936-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446212-T-A

135045945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446221-T-C

http://identifiers.org/hco/4/GRCh38#135045951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446227-C-A

135045951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446227-C-T

135045963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446239-T-C

http://identifiers.org/hco/4/GRCh38#135045964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446240-C-A

135045964-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446240-C-G

http://identifiers.org/hco/4/GRCh38#135045972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446248-C-A

135045973-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446249-A-T

135045990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446266-T-C

135046016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446293-T-C

135046016-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446293-T-G

135046038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446315-A-G

135046051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446328-A-G

135046074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446351-A-G

http://identifiers.org/hco/4/GRCh38#135046082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446359-C-A

135046082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446359-C-T

135046085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446362-G-A

135046085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446362-G-T

135046097-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446374-G-C

135046097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446374-G-T

135046107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446384-G-A

135046107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446384-G-T

135046113-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446390-T-A

135046113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446390-T-C

135046113-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446390-T-G

135046115-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446392-T-A

135046115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446392-T-C

135046118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446395-G-A

135046118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446395-G-T

135046126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446403-A-G

135046126-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446403-A-T

http://identifiers.org/hco/4/GRCh38#135046130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446407-C-A

135046130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446407-C-T

http://identifiers.org/hco/4/GRCh38#135046136-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446413-A-C

135046136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446413-A-G

135046136-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446413-A-T

http://identifiers.org/hco/4/GRCh38#135046141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446418-C-A

135046141-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446418-C-G

135046141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446418-C-T

135046142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446419-G-A

135046142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446419-G-T

http://identifiers.org/hco/4/GRCh38#135046143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446420-C-A

135046145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446422-G-A

135046145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446422-G-T

135046147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446424-T-C

135046154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446431-T-C

http://identifiers.org/hco/4/GRCh38#135046155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446432-C-A

135046155-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446432-C-G

http://identifiers.org/hco/4/GRCh38#135046160-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446437-C-A

135046160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446437-C-T

135046161-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446438-T-A

135046161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446438-T-C

http://identifiers.org/hco/4/GRCh38#135046167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446444-C-A

135046167-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446444-C-G

135046167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446444-C-T

135046179-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446456-T-G

http://identifiers.org/hco/4/GRCh38#135046182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446459-C-A

135046201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446478-G-A

135046201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446478-G-T

135046216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446493-A-G

135046216-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446493-A-T

http://identifiers.org/hco/4/GRCh38#135046248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446525-C-A

135046248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446525-C-T

135046256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446533-T-C

135046268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446545-T-C

135046269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446546-G-A

135046269-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446546-G-C

135046269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446546-G-T

http://identifiers.org/hco/4/GRCh38#135046281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446558-C-A

135046281-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446558-C-G

135046281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446558-C-T

http://identifiers.org/hco/4/GRCh38#135046310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446587-C-A

135046310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446587-C-T

135046343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446620-G-T

135046362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446639-G-A

135046408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446685-C-T

http://identifiers.org/hco/4/GRCh38#135046426-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446703-A-C

135046426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446703-A-G

135046432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446709-A-G

135046454-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446731-T-A

135046454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446731-T-C

http://identifiers.org/hco/4/GRCh38#135046529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446806-C-A

135046529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446806-C-T

135046597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446874-T-C

135046597-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446874-T-G

135046656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446934-G-A

135046656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446934-G-T

135046659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446937-G-A

135046659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446937-G-T

135046667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446945-T-C

135046667-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446945-T-G

135046671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446949-A-G

135046676-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446954-T-A

135046690-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446968-T-A

135046690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446968-T-C

135046693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446971-G-A

135046693-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446971-G-C

135046693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446971-G-T

135046700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446978-G-A

135046710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446988-G-A

135046715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446993-T-C

135046718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446996-A-G

http://identifiers.org/hco/4/GRCh38#135046720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446998-C-A

135046720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446998-C-T

135046721-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446999-T-A

135046721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446999-T-C

135046721-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40446999-T-G

http://identifiers.org/hco/4/GRCh38#135046722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40447000-C-A

135046722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40447000-C-T

135046724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40447002-G-T

http://identifiers.org/hco/4/GRCh38#135046730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40447008-C-A

135046730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40447008-C-T

135046745-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40447023-T-A

http://identifiers.org/hco/4/GRCh38#135046752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40447030-C-A

135046754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40447032-G-A

135046754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40447032-G-T

135046755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40447033-A-G

135046755-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40447033-A-T

http://identifiers.org/hco/4/GRCh38#135046756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40447034-C-A

135046756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40447034-C-T

http://identifiers.org/hco/4/GRCh38#135046763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40447041-C-A

135046763-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40447041-C-G

135046781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40447059-A-G

135046794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40447072-G-A

135046794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40447072-G-T

135046797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40447075-G-A

135046797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40447075-G-T

http://identifiers.org/hco/4/GRCh38#135046804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40447082-C-A

135046804-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40447082-C-G

135046804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40447082-C-T

135046807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40447085-G-A

135046807-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40447085-G-C

135046807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40447085-G-T

http://identifiers.org/hco/4/GRCh38#135046816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40447094-C-A

135046816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40447094-C-T

135046818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40447096-A-G

135046818-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40447096-A-T

135046819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40447097-A-G

135046819-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40447097-A-T

135046848-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40447126-T-A

135046848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37913
most severe consequence: non coding transcript exon variant
orthologous variants: 40447126-T-C