45777291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75768893-G-A

45777291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75768893-G-T

45777309-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75768875-T-G

45777310-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75768874-T-G

45777343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75768841-T-C

http://identifiers.org/hco/13/GRCh38#45777382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75768802-C-A

45777522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75768667-C-T

45777551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75768635-G-T

http://identifiers.org/hco/13/GRCh38#45777679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75768561-C-A

http://identifiers.org/hco/13/GRCh38#45777844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75768416-C-A

http://identifiers.org/hco/13/GRCh38#45778119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75767881-C-A

45778143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75767857-G-A

45778143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75767857-G-T

45778194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75767801-C-T

45778407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75767580-A-G

45778483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75767504-T-C

http://identifiers.org/hco/13/GRCh38#45778552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75767444-C-A

45778552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75767444-C-T

http://identifiers.org/hco/13/GRCh38#45778612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75767424-C-A

http://identifiers.org/hco/13/GRCh38#45778657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75767382-C-A

45779047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75767297-C-T

45779122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75767237-G-T

45779226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75767161-G-T

45779365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75767028-G-A

45779414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75767002-A-G

45779500-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75766927-T-G

http://identifiers.org/hco/13/GRCh38#45779558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75766877-C-A

45779558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75766877-C-T

45779694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75766775-A-G

45779694-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75766775-A-T

45779710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75766759-T-C

45780027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75766467-A-G

45780031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75766462-C-T

http://identifiers.org/hco/13/GRCh38#45780146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75766388-C-A

45780161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75766377-T-C

45780643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75766212-G-T

45780644-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75766211-G-C

http://identifiers.org/hco/13/GRCh38#45780663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75766192-C-A

45780717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75766123-G-T

45780785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75766064-T-C

http://identifiers.org/hco/13/GRCh38#45780852-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75766008-A-C

45780881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75765980-G-A

45780887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75765974-T-C

45781264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75765612-A-G

http://identifiers.org/hco/13/GRCh38#45781269-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75765607-C-A

45781269-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75765607-C-G

45781323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75765570-G-T

45781327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75765566-T-C

45781400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75765516-A-G

45781402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75765514-G-A

45781402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75765514-G-T

http://identifiers.org/hco/13/GRCh38#45781410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75765505-C-A

45781410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75765505-C-T

45781565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 75765364-C-T

http://identifiers.org/hco/13/GRCh38#45781566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#75765363-C-A

45781667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 75765265-T-C

45781817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 75765134-G-A

45782031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75764957-A-G

45782062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75764921-A-G

45782128-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75764858-G-T

45782131-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75764855-A-T

45782241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75764668-G-T

http://identifiers.org/hco/13/GRCh38#45782242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75764667-C-A

45782243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75764666-T-C

45782360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75764554-A-G

http://identifiers.org/hco/13/GRCh38#45782383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75764531-C-A

45782387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75764527-T-C

45782432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75764457-T-C

45782435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75764454-T-C

45782523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75764319-G-A

http://identifiers.org/hco/13/GRCh38#45782542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75764300-C-A

45782542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75764300-C-T

45782688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75764174-G-T

45782697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75764165-T-C

http://identifiers.org/hco/13/GRCh38#45782706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75764156-C-A

45782706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75764156-C-T

http://identifiers.org/hco/13/GRCh38#45782707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75764155-C-A

45782715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75764147-G-A

http://identifiers.org/hco/13/GRCh38#45782841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75764017-C-A

45782841-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75764017-C-G

45782877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75763986-G-A

45782885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75763978-T-C

45782932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75763954-A-G

45782949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75763938-G-A

45782949-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75763938-G-C

45782974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75763912-A-G

45782974-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75763912-A-T

45782975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75763911-G-T

45783083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75763803-G-T

45783091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75763795-A-G

http://identifiers.org/hco/13/GRCh38#45783293-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75763622-A-C

45783293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75763622-A-G

45783293-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75763622-A-T

45783305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75763610-G-A

45783305-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75763610-G-C

45783305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75763610-G-T

45783322-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75763599-A-T

45783326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75763595-G-T

http://identifiers.org/hco/13/GRCh38#45783368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75763571-C-A

45783368-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75763571-C-G

45783368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: 3 prime UTR variant
orthologous variants: 75763571-C-T

45783419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: synonymous variant
orthologous variants: 75763516-G-A

45783419-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: synonymous variant
orthologous variants: 75763516-G-C

45783419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: synonymous variant
orthologous variants: 75763516-G-T

45783447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: missense variant
orthologous variants: 75763488-C-T

45783591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: missense variant
orthologous variants: 75763344-T-C

45783615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: missense variant
orthologous variants: 75763320-G-A

45783663-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: missense variant
orthologous variants: 75763272-T-A

45783882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: missense variant
orthologous variants: 75763059-G-A

45783893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: synonymous variant
orthologous variants: 75763048-G-A

45783893-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: missense variant
orthologous variants: 75763048-G-C

45783893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: missense variant
orthologous variants: 75763048-G-T

45783895-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: missense variant
orthologous variants: 75763046-T-A

45783936-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: missense variant
orthologous variants: 75763005-T-G

45783961-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: missense variant
orthologous variants: 75762980-G-C

45784088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75762854-G-A

45784103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75762836-T-C

45784103-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75762836-T-G

http://identifiers.org/hco/13/GRCh38#45784105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75762834-C-A

45784110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75762829-C-T

45784125-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75762816-T-A

45784125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75762816-T-C

45784132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75762809-A-G

45784412-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75760467-T-A

45784412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75760467-T-C

45784412-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75760467-T-G

45784422-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75760457-G-C

45784422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75760457-G-T

45784454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75760423-G-T

45784474-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75760405-T-G

45784647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75760246-A-G

45784884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75760034-G-A

45784912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75760000-G-A

45784988-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75759929-A-T

45785038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75759879-A-G

45785061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75759856-G-A

45785133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75759787-A-G

45785139-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75759781-C-G

45785139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75759781-C-T

http://identifiers.org/hco/13/GRCh38#45785142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75759778-C-A

45785303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75759630-G-A

45785312-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75759621-T-A

45785506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75759461-T-C

45785897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75759082-T-C

45786503-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75758464-G-C

45787466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75756650-G-T

45787510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75756607-T-C

45787684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75756461-G-A

45787697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75756451-C-T

45787861-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75756292-G-C

45787880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75756274-C-T

http://identifiers.org/hco/13/GRCh38#45787894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75756260-C-A

45787967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75756187-T-C

45788117-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75756030-T-A

45788166-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75755981-T-A

45788166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75755981-T-C

45788445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75755704-G-A

45788445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75755704-G-T

45788642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75755499-G-A

45788673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75755468-A-G

http://identifiers.org/hco/13/GRCh38#45788674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75755467-C-A

45788674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75755467-C-T

45788908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75755264-G-A

45789498-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75754849-C-G

45789786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75754658-A-G

45789937-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75754505-A-T

45790067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75754394-C-T

45790179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75753475-G-A

45790179-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75753475-G-T

45790435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75753223-C-T

45790449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75753208-A-G

45790688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75752970-C-T

45790731-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75752941-A-T

45791586-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75752198-G-C

45791631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75752160-C-T

45791664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75752127-T-C

45793065-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75750662-T-G

45793481-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron_variant, undefined
orthologous variants: 75750021-T-A

45793481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron_variant, undefined
orthologous variants: 75750021-T-C

45793482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron_variant, undefined
orthologous variants: 75750020-G-T

45793540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75749966-G-A

45793666-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75749842-T-G

45793690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75749820-C-T

45794268-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75745363-G-C

http://identifiers.org/hco/13/GRCh38#45794286-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75745345-A-C

45794316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75745313-A-G

45794927-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75744769-G-C

45796283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75744224-G-A

45796297-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75744210-A-T

45796316-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75744191-T-A

45796425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75744113-A-G

45796466-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75744069-G-C

45796608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75743948-G-A

45796612-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75743944-T-G

45796908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75743723-G-A

45797031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75743606-T-C

45797141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75743499-T-C

45797168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75743479-A-G

45797168-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75743479-A-T

45797177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75743470-G-T

http://identifiers.org/hco/13/GRCh38#45797350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75743304-C-A

45797350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75743304-C-T

45797420-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75743242-C-G

45797452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75743211-C-T

45797971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75742749-T-C

45797988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75742735-C-T

45797989-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75742734-C-G

45798153-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75742568-T-G

45798200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75742521-A-G

45799441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75740417-G-A

45799450-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75740408-G-C

45799535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75740337-C-T

45799778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75740165-A-G

45799928-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75740018-C-G

45800334-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75739600-T-G

45800390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75739544-A-G

45800481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75739478-T-C

45800674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75739290-G-A

45800915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75739041-G-A

45801870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75737085-G-T

45801986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75736975-A-G

45802398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75736562-T-C

45804262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75734646-T-C

45804328-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75734580-T-A

45809119-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75732559-C-G

45809131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75732547-C-T

45809253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75732439-C-T

45809387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75732330-G-T

45809414-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75732303-G-C

45809666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75731711-G-A

45809821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75731574-G-A

45809838-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75731557-C-G

45809880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75731515-T-C

45809984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75731464-A-G

45810074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75731413-C-T

45810117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75731365-G-A

http://identifiers.org/hco/13/GRCh38#45810210-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75731274-A-C

45810245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75731240-C-T

45810594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75730906-G-A

45810654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75730865-G-T

45810691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75730832-A-G

45810715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75730808-T-C

45810847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75730686-G-T

45810849-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75730684-A-T

45810956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75730581-G-A

45810959-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75730578-A-T

45811231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75730294-T-C

http://identifiers.org/hco/13/GRCh38#45812158-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75729735-C-A

http://identifiers.org/hco/13/GRCh38#45812241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75729649-C-A

45812474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75729450-T-C

45812513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75729407-T-C

45812520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75729400-C-T

45812999-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75728927-T-A

45813007-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75728919-G-C

45813217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75728814-G-A

45813297-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75728776-T-G

45813434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75728632-G-A

45813575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75728522-T-C

45813810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75728279-A-G

45813924-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75728180-T-A

45813924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75728180-T-C

45814358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75728067-T-C

http://identifiers.org/hco/13/GRCh38#45814626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75727824-C-A

45814639-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75727811-A-T

45814689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75727762-T-C

45814689-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75727762-T-G

45815702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75726436-G-A

45815908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75726253-A-G

45815951-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75726210-C-G

45815954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75726207-A-G

45816069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75726092-A-G

45816336-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75725869-T-G

http://identifiers.org/hco/13/GRCh38#45816414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75725790-C-A

http://identifiers.org/hco/13/GRCh38#45816415-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75725789-A-C

45816421-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75725783-T-G

45816550-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75725656-T-A

45816639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75725583-C-T

45816700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75725531-T-C

45816729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75725503-C-T

45816819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75725419-G-T

45816838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75725400-A-G

45816923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75725328-G-A

45821812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75723595-C-T

45821827-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75723581-G-C

45821828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75723580-A-G

45821865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75723561-G-A

45821999-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75723456-C-G

45822012-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75723443-C-G

45822294-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75723214-A-T

45822994-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75722430-T-G

http://identifiers.org/hco/13/GRCh38#45823047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75722382-C-A

45823279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75722165-G-A

45823859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75721691-T-C

45824271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75721420-C-T

45824730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75720980-G-A

45824959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75720832-G-A

45825387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75720408-C-T

45825563-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75720201-T-G

45825912-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75719750-A-T

45826002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75719651-T-C

45826085-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75719581-G-C

45826383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75719135-G-A

45826393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75719126-A-G

45826393-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75719126-A-T

45826423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75719096-G-A

45826423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75719096-G-T

45827395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75719023-C-T

45827572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75718852-G-A

45827987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75718487-G-T

45828245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75718250-T-C

http://identifiers.org/hco/13/GRCh38#45828354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75718124-C-A

45828492-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75717991-C-G

45828497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75717986-A-G

45828576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75717906-T-C

http://identifiers.org/hco/13/GRCh38#45828678-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75717825-A-C

45828710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron_variant, undefined
orthologous variants: 75717794-T-C

45828895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron_variant, undefined
orthologous variants: 75717609-A-G

45828953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75717542-C-T

45829004-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75717491-T-G

45829188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75717317-A-G

45829256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75717249-C-T

45829274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75717231-C-T

http://identifiers.org/hco/13/GRCh38#45829685-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75717072-C-A

45829690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75717067-A-G

45829870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75716919-C-T

http://identifiers.org/hco/13/GRCh38#45830052-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75716772-A-C

45830090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75716725-C-T

45830138-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75716685-T-G

http://identifiers.org/hco/13/GRCh38#45830151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75716672-C-A

45830243-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75716588-G-C

45830345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75716479-G-A

45830712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75716138-G-A

45830802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75716047-A-G

45830941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75715939-G-A

45830941-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75715939-G-C

45831743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75715304-T-C

45831749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75715298-T-C

45831835-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75715212-G-C

45831869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75715178-G-A

45832039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75714657-C-T

45832068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75714623-G-A

45833479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75711440-G-A

45833647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75711297-G-A

http://identifiers.org/hco/13/GRCh38#45833655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75711290-C-A

45833655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75711290-C-T

45833707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75711233-C-T

45834007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron_variant, undefined
orthologous variants: 75710976-G-A

45835914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75709782-A-G

45836079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75709623-G-A

45836088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75709614-A-G

45836825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75709440-C-T

45837114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75709141-T-C

45837137-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75709119-T-G

45837144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75709112-T-C

45837154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75709102-A-G

45837154-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75709102-A-T

45837243-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75708797-G-C

45837253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75708787-T-C

45837404-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75708643-T-A

45837956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75707921-C-T

45838154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75707565-G-A

45838195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75707530-A-G

http://identifiers.org/hco/13/GRCh38#45838199-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75707526-A-C

45840421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75702139-T-C

45840527-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75702013-G-C

45840593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75701951-C-T

45840606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75701938-G-A

45840674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75701870-G-T

45840740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75701804-G-A

45841574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75700964-A-G

45841673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75700862-G-T

45841788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75700733-G-A

45841851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75700671-C-T

45846581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75698729-A-G

45846791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75698517-T-C

45846872-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75698437-C-G

45846874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75698435-G-A

http://identifiers.org/hco/13/GRCh38#45846970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75698346-C-A

45846998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75698317-A-G

45847142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75698178-T-C

45847331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75697989-A-G

45847407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75697853-T-C

45847661-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75697560-T-G

45847884-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75697312-C-G

45847884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75697312-C-T

45848053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75697167-T-C

http://identifiers.org/hco/13/GRCh38#45848094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75697133-C-A

45848122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75697116-C-T

45848597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75696695-G-A

45848665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75696637-A-G

45848869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75696468-T-C

45848930-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75696397-C-G

45848930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75696397-C-T

45849164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75696136-G-A

45849210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75696078-C-T

http://identifiers.org/hco/13/GRCh38#45849661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75695533-C-A

45849731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75695473-C-T

45849918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75695293-G-T

45850058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75695153-T-C

45850060-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75695151-G-C

45850077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75695134-A-G

45850302-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75694941-G-C

http://identifiers.org/hco/13/GRCh38#45850603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75694632-C-A

45850713-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75694536-G-C

45850713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75694536-G-T

45850765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75694470-G-A

http://identifiers.org/hco/13/GRCh38#45850883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75694346-C-A

http://identifiers.org/hco/13/GRCh38#45850921-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75694226-A-C

45850921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75694226-A-G

http://identifiers.org/hco/13/GRCh38#45850923-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75694224-A-C

45851103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75694047-G-A

45851103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75694047-G-T

45851259-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75693847-G-C

45851399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75693733-G-A

45851399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: intron variant
orthologous variants: 75693733-G-T

45851568-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30553
most severe consequence: missense variant
orthologous variants: 75693555-T-G