10896320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: 3 prime UTR variant
orthologous variants: 64058851-T-C

10896320-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: 3 prime UTR variant
orthologous variants: 64058851-T-G

http://identifiers.org/hco/8/GRCh38#10896350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#64058821-C-A

http://identifiers.org/hco/8/GRCh38#10896426-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#64058747-C-A

http://identifiers.org/hco/8/GRCh38#10896442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#64058729-C-A

10896442-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: 3 prime UTR variant
orthologous variants: 64058729-C-G

10896442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: 3 prime UTR variant
orthologous variants: 64058729-C-T

10896535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: 3 prime UTR variant
orthologous variants: 64058647-T-C

http://identifiers.org/hco/8/GRCh38#10896550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#64058639-C-A

10896555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: 3 prime UTR variant
orthologous variants: 64058634-A-G

10896558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: 3 prime UTR variant
orthologous variants: 64058631-C-T

10896582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: 3 prime UTR variant
orthologous variants: 64058607-T-C

10897131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: 3 prime UTR variant
orthologous variants: 64058081-C-T

10897207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: 3 prime UTR variant
orthologous variants: 64058006-G-T

10898673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: missense variant
orthologous variants: 64056516-A-G

10898805-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: missense variant
orthologous variants: 64056384-A-T

10898969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 64056221-G-A

10898969-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 64056221-G-C

10898995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, missense_variant
orthologous variants: 64056195-G-A

10898995-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, missense_variant
orthologous variants: 64056195-G-C

10898995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, missense_variant
orthologous variants: 64056195-G-T

10899080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64056117-T-C

10899116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64056083-A-G

http://identifiers.org/hco/8/GRCh38#10899121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#64056078-C-A

10899121-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64056078-C-G

10899121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64056078-C-T

10899757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64055939-T-C

10899818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64055881-C-T

http://identifiers.org/hco/8/GRCh38#10899999-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#64055694-A-C

10900046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64055651-G-A

10900340-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64055412-A-T

10900794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64054926-C-T

10900823-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64054898-G-C

10902468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64053982-C-T

10903472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64053055-G-A

10903909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64052381-G-A

10903909-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64052381-G-C

10903909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64052381-G-T

10904033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64052268-G-A

http://identifiers.org/hco/8/GRCh38#10904236-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#64052058-A-C

10904324-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64051987-G-C

10904324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64051987-G-T

10905367-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64050223-C-G

10905457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64050137-G-A

10905457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64050137-G-T

10905750-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64049871-A-T

10905766-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64049855-C-G

10906051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64049621-G-A

10906121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64049551-T-C

10906121-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64049551-T-G

http://identifiers.org/hco/8/GRCh38#10906232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#64049447-C-A

10906281-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64049378-A-T

10906283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64049376-C-T

10910791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64043075-C-T

10910881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64042980-G-A

http://identifiers.org/hco/8/GRCh38#10910928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#64042932-C-A

10911171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64042697-G-A

10911208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64042663-G-A

10911403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64042556-G-A

10911403-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64042556-G-C

http://identifiers.org/hco/8/GRCh38#10911465-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#64042515-A-C

http://identifiers.org/hco/8/GRCh38#10914508-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#64041764-A-C

10914508-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64041764-A-T

http://identifiers.org/hco/8/GRCh38#10914557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#64041718-C-A

10914723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64041562-T-C

10914945-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64041345-G-C

10915070-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64041248-G-C

10915171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64041160-T-C

10915338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64040996-G-A

10915339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64040995-T-C

10915377-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64040955-C-G

10915502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64040835-T-C

10915543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64040808-T-C

10915563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64040790-G-A

10915721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64040639-G-T

10915792-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64040554-G-C

10916018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64040375-T-C

http://identifiers.org/hco/8/GRCh38#10916041-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#64040353-A-C

10916041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64040353-A-G

10916073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64040329-T-C

10916148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64040263-G-A

10916148-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64040263-G-C

10916177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64040241-G-A

10916533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64039647-G-T

10916535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64039645-G-A

10916623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64039570-G-A

10916687-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64039502-G-T

10916715-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64039474-A-T

10916732-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64039457-T-A

10916739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64039450-G-A

http://identifiers.org/hco/8/GRCh38#10916796-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#64039395-A-C

10916815-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64039369-T-G

http://identifiers.org/hco/8/GRCh38#10916830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#64039358-C-A

10916830-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64039358-C-G

10917108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64038665-C-T

10917266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64038518-T-C

10917335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64038451-T-C

10917506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64038134-G-A

10917506-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64038134-G-C

10924034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64036699-G-T

10924530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64035971-G-A

10924530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64035971-G-T

http://identifiers.org/hco/8/GRCh38#10924531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#64035970-C-A

10924531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64035970-C-T

10924543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64035955-A-G

10924544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64035954-G-A

10924544-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64035954-G-C

10924544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64035954-G-T

10924557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64035941-G-A

10924557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64035941-G-T

10924587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64035907-G-A

10924587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64035907-G-T

10924608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64035886-G-A

10924618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64035866-G-A

10924618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64035866-G-T

10924842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64035642-G-T

10924894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64035588-T-C

http://identifiers.org/hco/8/GRCh38#10924906-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#64035576-A-C

10924906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64035576-A-G

10924962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64035518-T-C

10924962-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64035518-T-G

10924966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64035514-A-G

10925320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64035209-A-G

10925334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64035201-A-G

10925337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64035198-G-A

10925413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64035125-C-T

10925574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64034960-T-C

10925612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64034920-G-A

10925775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64034801-C-T

10926123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64034548-T-C

10928592-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64032851-C-G

10928701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64032741-G-A

10929020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64032468-G-A

10929040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64032455-G-A

10929040-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64032455-G-C

http://identifiers.org/hco/8/GRCh38#10929168-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#64032313-A-C

10939283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64029810-C-T

10939397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64029683-G-A

10939440-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64029640-G-C

10939440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64029640-G-T

10939442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64029638-T-C

10940356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64028319-G-A

10940451-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64028241-G-C

10940469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64028223-A-G

10940620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64028065-C-T

10940796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64027926-C-T

10940797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64027925-G-A

10940838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64027887-T-C

10940927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64027764-G-T

10940987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64027707-T-C

http://identifiers.org/hco/8/GRCh38#10941339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#64027484-C-A

10941339-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64027484-C-G

10941339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64027484-C-T

10941436-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64027382-G-C

10941625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64027190-G-A

10941647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64027168-G-A

10941647-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64027168-G-C

10941661-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64027153-C-G

10941897-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64026878-T-A

10942179-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64026551-G-C

10942275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64026394-G-T

http://identifiers.org/hco/8/GRCh38#10942332-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#64026274-A-C

10942466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64026148-A-G

10944034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64025258-C-T

10944100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64025177-A-G

10944310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64024995-A-G

10944380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64024963-C-T

10944435-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64024917-G-C

10944446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64024906-A-G

10944446-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64024906-A-T

http://identifiers.org/hco/8/GRCh38#10944576-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#64024802-A-C

http://identifiers.org/hco/8/GRCh38#10944607-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#64024771-C-A

10944607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64024771-C-T

10944654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64024719-A-G

10944701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64024667-A-G

10949582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64023725-G-A

10949609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64023702-C-T

10949954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64023460-A-G

10950086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64023403-T-C

10950143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64023361-G-A

10950307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64023217-C-T

10950339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64023172-A-G

10950345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64023150-C-T

10950399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64023091-G-T

http://identifiers.org/hco/8/GRCh38#10950638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#64022875-C-A

10950638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64022875-C-T

10950670-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64022841-C-G

10950670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64022841-C-T

10950695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64022816-C-T

10950752-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64022760-T-G

10950864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64022667-T-C

http://identifiers.org/hco/8/GRCh38#10951098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#64022472-C-A

10951258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64022321-G-A

10951360-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64022259-G-C

10951360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64022259-G-T

10951391-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64022228-C-G

10951618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64022025-T-C

10951925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64021740-C-T

10952075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64021610-C-T

http://identifiers.org/hco/8/GRCh38#10955404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#64018521-C-A

10955404-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64018521-C-G

10955533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64018413-G-A

10955617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64018312-G-T

10955763-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64018191-T-G

10957530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64017353-G-T

10957636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64017252-G-A

10957636-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64017252-G-C

http://identifiers.org/hco/8/GRCh38#10957648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#64017240-C-A

10957649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64017239-C-T

10958043-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64016896-T-G

10958044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64016895-T-C

10959860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64015141-A-G

10961361-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64014012-G-C

10961433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64013943-G-A

10961468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64013908-G-A

10961972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64013055-T-C

http://identifiers.org/hco/8/GRCh38#10962168-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#64012868-A-C

10962324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64012725-C-T

10962940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64012514-A-G

10962972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64012482-T-C

http://identifiers.org/hco/8/GRCh38#10965400-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#64011326-A-C

10965414-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64011312-G-C

10965456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64011278-A-G

10965830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64010934-A-G

10965942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64010816-G-A

10966038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64010762-G-A

10966038-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64010762-G-C

http://identifiers.org/hco/8/GRCh38#10977120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#64009142-C-A

10977178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64009090-C-T

10977262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64009028-T-C

10977318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, undefined
orthologous variants: 64008990-A-G

10977374-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, undefined
orthologous variants: 64008936-C-G

10977481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64008841-G-T

10977590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64008757-G-A

10977592-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64008755-G-C

10977623-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64008725-T-G

10977777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64008631-C-T

10977791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64008621-C-T

10977915-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64008557-T-G

http://identifiers.org/hco/8/GRCh38#10977929-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#64008543-A-C

10978114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64008366-G-A

10978144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64008346-G-A

10978901-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64007343-G-C

10979167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64007088-G-A

10979178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64007077-T-C

10979625-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64006711-G-C

10979812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64006557-T-C

10979915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64006470-T-C

10979988-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64006415-G-C

10980278-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64006233-G-C

10980321-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64006196-C-G

10980374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64006144-G-A

10981178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64005526-A-G

10981199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64005499-G-A

10981327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64005364-G-A

10981416-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64005287-G-C

10981416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64005287-G-T

10981470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64005225-G-A

10981470-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64005225-G-C

10981519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64005174-T-C

10981595-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64005083-G-C

10981631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64005050-C-T

10981632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64005049-G-A

10981853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64004822-G-A

10982021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64004722-G-A

10982750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64004060-G-A

10982775-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64004039-T-A

10983234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64003218-G-T

10983448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 64002868-A-G

10987100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63999299-T-C

10987100-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63999299-T-G

10987152-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63999251-T-A

10987214-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63999189-G-C

10988459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63997877-A-G

10988612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63997767-C-T

10988631-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63997746-G-C

10988690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63997686-G-A

10988690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63997686-G-T

10988759-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63997633-T-A

10988780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63997610-C-T

10988800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63997590-A-G

10989093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63997366-G-A

10989093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63997366-G-T

10989170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63997314-G-T

10989304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63997166-T-C

10989334-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63997142-A-T

10989379-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63997098-A-T

10989453-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63997037-T-A

10989466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63997024-A-G

10989646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63996869-C-T

10991150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63996053-T-C

10991328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, undefined
orthologous variants: 63995882-G-A

10991432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63995784-G-A

10991441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63995775-T-C

10991467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63995749-G-T

10991468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63995748-G-T

10991726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63995490-G-T

10991893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63995326-T-C

10991938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63995280-T-C

10992264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63994951-G-A

10992289-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63994910-A-T

10992291-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63994908-A-T

10992308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63994891-T-C

10992375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63994782-G-A

10992450-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63994707-T-G

10992572-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63994580-T-A

http://identifiers.org/hco/8/GRCh38#10992777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63994375-C-A

10992958-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63994195-C-G

10993005-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63994144-T-G

10993196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63993961-G-A

10993347-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63993811-G-C

10993510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63993641-G-A

10993649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63993508-C-T

http://identifiers.org/hco/8/GRCh38#10993843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63993331-C-A

10994041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63993173-G-A

http://identifiers.org/hco/8/GRCh38#10994087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63993122-C-A

10994571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63992690-G-A

10994573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63992688-C-T

http://identifiers.org/hco/8/GRCh38#10994691-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63992574-A-C

10994857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63992440-C-T

10995987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63989126-A-G

10995987-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63989126-A-T

10996026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63989080-G-A

10996104-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63989008-G-C

10996156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63988960-A-G

10996156-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63988960-A-T

10996324-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63988813-C-G

10996324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63988813-C-T

10996719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63988397-A-G

10996736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63988351-G-A

10997002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63988049-T-C

10997033-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63987984-A-T

10997054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63987963-G-A

10997054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63987963-G-T

10997125-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63987895-C-G

http://identifiers.org/hco/8/GRCh38#10997765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63986851-C-A

10997917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63986727-A-G

10997988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63986657-T-C

10998064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63986597-G-A

10998152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63986575-G-A

10998286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63986447-C-T

http://identifiers.org/hco/8/GRCh38#10998301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63986432-C-A

10998730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63986013-C-T

10999000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63985833-T-C

10999002-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63985831-G-C

10999198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63985638-C-T

10999338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63985492-A-G

11012054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63984494-G-A

11012784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63983927-C-T

11012814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63983897-G-T

11013012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63983736-T-C

11013180-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63983569-A-T

http://identifiers.org/hco/8/GRCh38#11013555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63983199-C-A

11013778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63983000-G-A

11013778-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63983000-G-C

11013858-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63982930-C-G

11014222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63982561-T-C

11014468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63982314-C-T

11014496-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63982283-G-C

11014503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63982276-C-T

11014704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63982089-C-T

11016826-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63980700-G-C

11017303-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63980317-G-C

11017334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63980286-A-G

http://identifiers.org/hco/8/GRCh38#11017418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63980229-C-A

11017418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63980229-C-T

11017508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63980134-G-A

11017508-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63980134-G-C

11017580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63980041-G-A

11017914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63979204-T-C

11018190-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63978964-T-A

11018190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63978964-T-C

11018193-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63978961-G-C

11018204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63978950-C-T

http://identifiers.org/hco/8/GRCh38#11018220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63978931-C-A

11018222-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63978929-C-G

11018265-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63978898-C-G

11018363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63978806-T-C

11018642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63977802-G-T

http://identifiers.org/hco/8/GRCh38#11018888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63976689-C-A

11019128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63976459-G-A

11020199-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63976088-G-C

11021215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63975476-C-T

11021508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63975203-G-A

11021508-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63975203-G-C

11022808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63973504-G-T

11022833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63973479-T-C

http://identifiers.org/hco/8/GRCh38#11023757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63972709-C-A

11025323-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63972112-T-G

11025452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63971985-A-G

11025493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63971946-T-C

11025615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63971835-C-T

11025629-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63971821-T-A

11025695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63971751-G-A

11025695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63971751-G-T

11025745-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63971701-T-A

11025761-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63971685-A-T

11028876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63971351-G-A

11028900-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63971326-G-C

11028946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63971286-C-T

11029072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63971127-G-A

11029106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63971107-C-T

11029319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63970881-C-T

11029890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63970707-G-A

11030027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63970602-G-A

11030106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63970545-G-A

11030106-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63970545-G-C

11030128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63970523-C-T

http://identifiers.org/hco/8/GRCh38#11030155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63970510-C-A

11030184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63970479-C-T

11030805-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63969255-C-G

11030805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63969255-C-T

11030806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63969254-C-T

11031000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63969002-T-C

11031182-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63968767-A-T

11031183-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63968766-T-A

11031183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63968766-T-C

11031232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63968732-G-A

11031240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63968725-G-A

11031357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63968634-T-C

11031458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63968545-C-T

11031610-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63968350-T-G

11031640-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63968317-G-C

11031794-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63968175-A-T

11031805-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63968164-T-A

11031805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63968164-T-C

11031873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63968068-C-T

11032321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63967645-T-C

11032438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63967511-G-A

http://identifiers.org/hco/8/GRCh38#11032512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63967435-C-A

http://identifiers.org/hco/8/GRCh38#11032682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63967283-C-A

11032750-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63967146-A-T

11032855-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63966987-T-G

11032861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63966981-G-A

11032889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63966956-G-T

11032978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63966886-A-G

11033039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63966859-T-C

11033107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63966816-G-A

11033107-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63966816-G-C

11033318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63966709-G-A

11033336-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63966691-G-C

11033349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63966678-A-G

11033485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63966582-T-C

11033486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63966581-G-A

11033574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63966532-G-A

11033578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63966528-T-C

11033600-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63966515-C-G

11033604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63966511-C-T

11033665-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63966450-A-T

11033826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63966307-A-G

11034003-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63966137-C-G

11034010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63966130-C-T

11034027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63966112-T-C

11034103-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63966031-T-A

http://identifiers.org/hco/8/GRCh38#11034123-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63966001-A-C

11034174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63965966-G-T

11034317-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63965844-G-C

11034342-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63965821-A-T

11034366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63965810-A-G

11034577-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63965711-T-A

11034727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63965575-T-C

11034748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63965555-T-C

11034791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63965514-C-T

11034881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63965424-A-G

11034948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63965361-C-T

11035125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63964788-G-A

11035125-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63964788-G-C

11035136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63964777-G-A

11035136-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63964777-G-C

11035136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63964777-G-T

11035351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63964573-C-T

http://identifiers.org/hco/8/GRCh38#11035404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63964547-C-A

11035404-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63964547-C-G

11035564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63964407-T-C

11035806-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63964128-T-G

11035819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63964115-C-T

11035856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63964086-T-C

11035870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63964072-T-C

11036355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63963933-C-T

http://identifiers.org/hco/8/GRCh38#11036365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63963923-C-A

11036366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63963922-C-T

11036440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63963851-T-C

11036450-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63963841-G-C

11036533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63963768-T-C

11036571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63963728-G-A

11036571-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63963728-G-C

11048296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, undefined
orthologous variants: 63959749-A-G

11048309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, undefined
orthologous variants: 63959736-G-A

11048366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, undefined
orthologous variants: 63959700-G-A

11048366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, undefined
orthologous variants: 63959700-G-T

11053258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63956693-G-A

11053454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63956529-G-A

11053454-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63956529-G-C

11053510-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, undefined
orthologous variants: 63956477-G-C

http://identifiers.org/hco/8/GRCh38#11053576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#63956381-C-A

11053830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63956094-A-G

11054288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63955636-G-A

11054288-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63955636-G-C

11054521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63955385-G-A

11054663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63955265-C-T

11054687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63955241-A-G

11055082-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63954893-C-G

11055146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63954852-A-G

11055146-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63954852-A-T

http://identifiers.org/hco/8/GRCh38#11055203-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63954813-A-C

11055293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63954739-G-A

11055325-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63954709-T-A

11055583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63954554-G-A

11056126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63954115-G-T

11056130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63954111-G-A

11056130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63954111-G-T

11056514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63953796-T-C

11056520-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63953790-T-A

11059477-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63952253-C-G

11059524-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63952199-G-C

11059564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63952158-G-A

11059564-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63952158-G-C

11059664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63952096-G-A

11059671-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63952089-C-G

11059792-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63951994-T-A

11059819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63951967-A-G

11060821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63951411-G-A

11060900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63951335-T-C

11061681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63950568-A-G

11061690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63950559-G-A

11061691-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63950558-A-T

11061726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63950520-G-A

11061886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63950354-G-A

http://identifiers.org/hco/8/GRCh38#11062149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63950086-C-A

http://identifiers.org/hco/8/GRCh38#11062530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63949767-C-A

11062530-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63949767-C-G

11062598-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63949722-T-G

11062674-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63949651-T-A

11062674-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63949651-T-G

11062682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63949645-T-C

11062730-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63949602-A-T

11062731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63949601-T-C

http://identifiers.org/hco/8/GRCh38#11063623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63949019-C-A

11063683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63948971-T-C

11063834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63948811-G-A

11063834-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63948811-G-C

11063939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63948680-A-G

11063966-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63948653-C-G

11063990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63948635-T-C

11064053-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63948575-C-G

11064053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63948575-C-T

11064084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63948543-A-G

11064114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63948513-G-A

http://identifiers.org/hco/8/GRCh38#11064915-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63947301-A-C

11064918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63947298-T-C

11064919-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63947297-C-G

11065199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63947030-C-T

11065233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63947001-T-C

11065398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63946735-G-A

11065413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63946720-T-C

11065413-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63946720-T-G

11065436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63946697-G-A

11065579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63946462-C-T

11065580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63946461-G-A

11065580-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63946461-G-C

11068138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63944175-T-C

11068249-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63944068-G-C

11068286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63944016-A-G

11068286-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63944016-A-T

11068348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63943967-G-A

11068348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63943967-G-T

11068385-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63943931-A-T

11068388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63943928-G-A

11068415-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63943902-T-A

11068653-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63943665-T-G

11068731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63943547-G-A

11068774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63943506-A-G

11068879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63943344-G-A

11068884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63943339-G-A

11068898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63943324-C-T

11069055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63943161-T-C

11069372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63942802-C-T

11069450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63942725-C-T

11069573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63942655-A-G

11069661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63942571-G-A

11069704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63942533-G-A

11069704-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63942533-G-C

11072051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63941614-T-C

http://identifiers.org/hco/8/GRCh38#11072119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63941547-C-A

11072119-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63941547-C-G

11072633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, undefined
orthologous variants: 63941275-G-A

11072700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, undefined
orthologous variants: 63941222-C-T

11073401-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63940899-G-C

11073837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63940468-G-A

11073847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63940458-G-T

11073899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63940406-G-A

11073899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63940406-G-T

11074008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63940313-A-G

http://identifiers.org/hco/8/GRCh38#11074009-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63940312-A-C

11074061-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63940266-T-A

11074090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63940237-G-T

11074117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63940209-G-A

11074117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63940209-G-T

11074291-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63940012-G-C

11074312-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63939991-C-G

11074713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63939538-T-C

11074822-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63939432-A-T

11074835-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63939417-T-G

11074840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63939413-G-A

11074852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63939401-T-C

11074916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63939337-G-A

11075021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63939279-G-A

11075037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63939263-C-T

http://identifiers.org/hco/8/GRCh38#11075157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63939170-C-A

11075217-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63939111-G-C

11075217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63939111-G-T

11075262-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63939040-G-T

http://identifiers.org/hco/8/GRCh38#11075977-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63938149-A-C

11075977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63938149-A-G

11076120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63938015-C-T

http://identifiers.org/hco/8/GRCh38#11076381-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63937763-A-C

11076381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63937763-A-G

11076498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63937643-G-A

11076498-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63937643-G-C

11077216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63937278-C-T

11077236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63937255-G-A

11077343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63937177-T-C

11077377-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63937144-G-C

11077542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63936979-G-A

11077542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63936979-G-T

11078053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63936508-G-A

11078419-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63936162-C-G

11078419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63936162-C-T

11078684-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63935923-C-G

11078821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63935804-C-T

11079209-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63935454-G-C

11079235-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63935429-G-C

11079411-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63935272-G-C

11079509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63935191-T-C

11079613-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63935093-C-G

11080862-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63933468-T-A

11080862-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63933468-T-G

11080964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63933367-G-A

11080964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63933367-G-T

11081088-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63932863-T-G

11081124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63932803-T-C

11081160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63932763-T-C

11081160-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63932763-T-G

11081281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63932651-A-G

11081316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63932616-C-T

11081483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63932450-C-T

11081590-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63932343-G-C

11084081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63930791-G-A

http://identifiers.org/hco/8/GRCh38#11084219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63930680-C-A

11084219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63930680-C-T

11084220-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63930679-T-A

11084331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63930570-T-C

11084423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63930494-G-A

11085162-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63929769-G-C

11085247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63929698-G-T

11085350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63929637-G-A

11085419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63929588-T-C

11085424-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63929583-G-C

11086057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63928809-T-C

11086057-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63928809-T-G

11086150-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63928733-T-A

11086151-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63928732-T-A

11086152-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63928731-T-A

11086153-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63928730-T-A

11086154-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63928729-T-A

11086155-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63928728-T-A

http://identifiers.org/hco/8/GRCh38#11086206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63928677-C-A

11086354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63928583-G-T

11086417-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63928510-C-G

11086417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63928510-C-T

11086668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63928272-T-C

11087197-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63927868-G-C

11087397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63927713-C-T

11088289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63921940-C-T

11089081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63920803-T-C

11089081-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63920803-T-G

11089114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63920770-C-T

11092454-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63919329-C-G

11092454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63919329-C-T

11092509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63919274-T-C

11092511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63919272-G-A

11092521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63919262-T-C

11092571-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63919192-G-C

11094603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63917068-T-C

11094796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63916888-C-T

11094815-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63916871-T-G

11095345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63916380-T-C

11095565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63916213-C-T

11095686-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63916088-T-A

11098588-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63915141-T-A

11098613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63915116-T-C

http://identifiers.org/hco/8/GRCh38#11098817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63914842-C-A

11098840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63914805-T-C

11098846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63914789-G-A

11099062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63914499-G-A

11099281-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63914344-C-G

11099335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63914290-G-T

11099346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63914279-G-A

http://identifiers.org/hco/8/GRCh38#11100556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63908728-C-A

11100556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63908728-C-T

11100924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63908453-T-C

11101094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63908363-C-T

11101143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63908313-G-A

11101143-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63908313-G-C

11102326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63906967-T-C

11102326-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63906967-T-G

http://identifiers.org/hco/8/GRCh38#11102473-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63906851-A-C

11102486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63906838-A-G

11102512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63906813-A-G

11102616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63906709-C-T

11102831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63906585-G-A

11103194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63906209-C-T

11103390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63906041-C-T

11103438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63906008-T-C

11103859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63905602-T-C

11104130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63905355-T-C

http://identifiers.org/hco/8/GRCh38#11104146-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63905340-A-C

http://identifiers.org/hco/8/GRCh38#11104215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63905277-C-A

http://identifiers.org/hco/8/GRCh38#11104408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63905115-C-A

11104408-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63905115-C-G

11104426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63905097-C-T

11104526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63904999-G-A

11104677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63904879-T-C

http://identifiers.org/hco/8/GRCh38#11104682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63904874-C-A

11104793-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63904713-G-C

11104793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63904713-G-T

11104815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63904667-G-A

11104815-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63904667-G-C

11104815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63904667-G-T

11104858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63904623-G-T

11104905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63904583-T-C

11104905-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63904583-T-G

11105297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63904268-G-A

11105297-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63904268-G-C

11105297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63904268-G-T

11105299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63904266-G-A

11105299-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63904266-G-C

11105300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63904265-A-G

11105697-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63903866-G-C

http://identifiers.org/hco/8/GRCh38#11105763-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63903800-A-C

11105913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63903672-A-G

http://identifiers.org/hco/8/GRCh38#11106178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63903449-C-A

11106178-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63903449-C-G

http://identifiers.org/hco/8/GRCh38#11106270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63903369-C-A

11106270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63903369-C-T

11106374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63903307-T-C

http://identifiers.org/hco/8/GRCh38#11106401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63903283-C-A

11106564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63903168-G-A

11106564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63903168-G-T

http://identifiers.org/hco/8/GRCh38#11106565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63903167-C-A

11106565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63903167-C-T

11108434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63902474-A-G

11108458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63902458-T-C

11108519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63902397-C-T

http://identifiers.org/hco/8/GRCh38#11108860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63902156-C-A

11108920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63902098-T-C

http://identifiers.org/hco/8/GRCh38#11108966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63902088-C-A

11109090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63901989-C-T

11109118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63901963-C-T

11109231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63901916-A-G

11109302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63901848-A-G

http://identifiers.org/hco/8/GRCh38#11109466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63901683-C-A

http://identifiers.org/hco/8/GRCh38#11109473-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63901676-C-A

http://identifiers.org/hco/8/GRCh38#11109527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63901619-C-A

11109527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63901619-C-T

11109535-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63901611-C-G

http://identifiers.org/hco/8/GRCh38#11109634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63901541-C-A

11109634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63901541-C-T

11109646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63901529-T-C

11111418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63900502-G-A

11111612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: intron variant
orthologous variants: 63900289-G-A

11111765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63900156-C-T

11111793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63900129-G-A

11111833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63900089-A-G

11111967-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63899954-T-A

11111967-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63899954-T-G

11112144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63899798-T-C

11112144-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63899798-T-G

11113054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63898717-T-C

11113086-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63898685-T-A

http://identifiers.org/hco/8/GRCh38#11114206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63898155-C-A

11114206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63898155-C-T

11114279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63898084-T-C

http://identifiers.org/hco/8/GRCh38#11114290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63898070-C-A

11114305-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63898055-G-C

http://identifiers.org/hco/8/GRCh38#11114314-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63898046-A-C

11122104-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63897046-G-C

11122427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63896766-C-T

11124627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63892146-A-G

11124676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63892100-A-G

11125378-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63891864-G-C

11125392-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63891850-G-C

11126602-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63888922-C-G

11126784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63888802-C-T

11126822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63888776-G-A

11129502-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63879643-G-C

11129539-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63879612-T-A

11130925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63878951-A-G

11130959-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63878917-G-C

11130992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63878884-T-C

11131058-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63878816-G-C

11131309-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63878597-G-C

11131390-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63878511-T-A

11131390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63878511-T-C

http://identifiers.org/hco/8/GRCh38#11131408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63878493-C-A

11131408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63878493-C-T

11138977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63876406-C-T

11139017-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63876366-T-A

http://identifiers.org/hco/8/GRCh38#11150867-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63872401-A-C

11150877-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63872391-T-A

11150991-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63872281-T-A

http://identifiers.org/hco/8/GRCh38#11151606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63871406-C-A

11151606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63871406-C-T

11151650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63871374-T-C

11151741-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63871286-C-G

11151744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63871283-G-A

11152046-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63871023-A-T

11152147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63870749-T-C

11152341-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63870634-G-C

11152589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63870457-A-G

http://identifiers.org/hco/8/GRCh38#11152745-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63870337-A-C

11152829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63870266-C-T

11155073-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63869401-T-A

11155321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63869214-G-A

11155321-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63869214-G-C

11158022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63865355-A-G

11158107-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63865263-C-G

11158421-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63865007-C-G

http://identifiers.org/hco/8/GRCh38#11158528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63864911-C-A

11158528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63864911-C-T

11158537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63864901-A-G

11158570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63864885-T-C

11158616-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63864848-C-G

11158757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63864753-G-A

11158757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63864753-G-T

11158858-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63864691-T-A

11158949-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63864602-T-A

11158949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63864602-T-C

11163051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63863667-T-C

11163275-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63863459-T-A

11163275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63863459-T-C

11163362-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63863342-G-C

11163362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63863342-G-T

11163424-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63863299-G-C

11163457-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63863265-C-G

11163611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63863139-T-C

11163690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63863044-C-T

http://identifiers.org/hco/8/GRCh38#11163965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63862809-C-A

11164559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63862257-T-C

11164612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63862176-C-T

http://identifiers.org/hco/8/GRCh38#11164805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63862022-C-A

11165017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63861840-G-A

11165017-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63861840-G-C

http://identifiers.org/hco/8/GRCh38#11165523-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63861649-A-C

11165528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63861644-G-A

11166260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63859960-T-C

11167136-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63859155-C-G

11167136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63859155-C-T

11167362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63858952-T-C

11167702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63858623-G-A

11167751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63858576-C-T

http://identifiers.org/hco/8/GRCh38#11167929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63858292-C-A

11168005-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63858218-G-C

11168072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63858130-C-T

11168158-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63858052-A-T

11172649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63857448-G-A

11174207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63856137-G-A

11174295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63856071-G-A

11174444-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63855937-G-C

11174732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63855655-G-A

11174749-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63855637-C-G

11174887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63855492-A-G

11174937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63855453-T-C

11176034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63854895-T-C

11176042-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63854887-T-G

11184151-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63854787-G-C

11184246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63854709-T-C

11184546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63854482-T-C

11184582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63854446-G-T

11185630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63854146-G-A

11185779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63854016-C-T

http://identifiers.org/hco/8/GRCh38#11186881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63852454-C-A

11187215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63852137-G-T

http://identifiers.org/hco/8/GRCh38#11187240-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63852111-A-C

11187240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63852111-A-G

11187275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63852076-T-C

11187850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63851486-C-T

11187944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63851413-G-A

11190746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63849730-A-G

11190859-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63849557-T-A

11190859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63849557-T-C

11191103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63849341-T-C

11197378-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63849252-A-T

11198340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63847817-C-T

11198433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63847725-T-C

11198869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63847240-G-A

11198983-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63847015-G-C

11199210-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63846810-G-C

11199211-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63846809-G-C

11199635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63846425-A-G

11199789-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63845472-G-C

11199975-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63845305-A-T

11199993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63845284-T-C

11200317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63844950-G-A

11200328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63844939-G-A

11200328-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63844939-G-C

11200335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63844932-G-T

11200430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63844841-T-C

11200430-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63844841-T-G

11200431-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63844840-T-G

11200503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63844775-G-A

http://identifiers.org/hco/8/GRCh38#11200645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63844662-C-A

11200645-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63844662-C-G

11200645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63844662-C-T

11200774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 63844533-G-A

11200774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 63844533-G-T

11200936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63844371-G-A

11201098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 63844212-T-C

11201098-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 63844212-T-G

11201166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 63844144-G-A

11201166-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63844144-G-C

11201166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63844144-G-T

11201176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63844134-T-C

11201388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 63843934-G-A

11201388-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 63843934-G-C

11201388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 63843934-G-T

11201456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63843867-G-A

11201633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63843693-G-A

11201633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27806
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63843693-G-T