29700369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: 37897651-G-A

29700409-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: 37897612-C-G

http://identifiers.org/hco/19/GRCh38#29700423-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#37897598-A-C

29700473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: 37897562-G-T

29700490-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: 37897545-T-G

29700521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: 37897496-T-C

29700521-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: 37897496-T-G

29700523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: 37897494-C-T

29700531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: 37897480-G-A

29700531-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: 37897480-G-C

http://identifiers.org/hco/19/GRCh38#29700591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#37897433-C-A

http://identifiers.org/hco/19/GRCh38#29700607-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#37897420-C-A

29700607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: 37897420-C-T

http://identifiers.org/hco/19/GRCh38#29700611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#37897418-C-A

29700611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: 37897418-C-T

http://identifiers.org/hco/19/GRCh38#29700615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#37897414-C-A

29700615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: 37897414-C-T

29700702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: 37897374-A-G

29700724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: 37897349-C-T

29700772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: 37897313-A-G

29700832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: 37897266-A-G

29700856-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: 37897243-T-A

29700856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: 37897243-T-C

29700875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: 37897224-A-G

29700885-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: 37897203-C-G

http://identifiers.org/hco/19/GRCh38#29700894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#37897195-C-A

http://identifiers.org/hco/19/GRCh38#29700899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#37897190-C-A

29700962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: 37897128-G-T

http://identifiers.org/hco/19/GRCh38#29701011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#37897107-C-A

29701011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: 37897107-C-T

http://identifiers.org/hco/19/GRCh38#29701012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#37897106-C-A

29701016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: 37897102-A-G

29701020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: 37897098-G-A

29701020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: 37897098-G-T

29701031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: 37897097-A-G

http://identifiers.org/hco/19/GRCh38#29701042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#37897086-C-A

29702026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: 37895020-G-A

29702087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: 37894939-G-A

29702097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: 37894930-G-A

29702116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: 37894914-G-A

29702118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: 37894912-G-T

29702123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: 37894907-A-G

29702155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: 37894875-G-T

29702161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: 37894869-C-T

29702177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: 37894853-G-T

http://identifiers.org/hco/19/GRCh38#29702192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#37894838-C-A

29702200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: 37894830-G-A

29702200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: 37894830-G-T

29702202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: 37894828-G-A

http://identifiers.org/hco/19/GRCh38#29702203-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#37894827-A-C

29702203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: 37894827-A-G

29702210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: 37894820-C-T

29702212-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: 37894818-C-G

29702212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: 37894818-C-T

http://identifiers.org/hco/19/GRCh38#29702260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#37894769-C-A

29702266-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: 37894763-G-C

http://identifiers.org/hco/19/GRCh38#29702273-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#37894756-A-C

29702273-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: 37894756-A-T

29702285-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: 37894751-T-A

29702285-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: 37894751-T-G

29702323-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: 37894717-C-G

http://identifiers.org/hco/19/GRCh38#29702377-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#37894678-A-C

29702377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: 37894678-A-G

29702377-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: 37894678-A-T

29702385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: 37894670-C-T

http://identifiers.org/hco/19/GRCh38#29702403-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#37894653-C-A

29702403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: 37894653-C-T

http://identifiers.org/hco/19/GRCh38#29702435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#37894618-C-A

29702435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: 37894618-C-T

29702453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: 37894600-T-C

29702453-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: 37894600-T-G

http://identifiers.org/hco/19/GRCh38#29702463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#37894590-C-A

http://identifiers.org/hco/19/GRCh38#29702487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#37894568-C-A

http://identifiers.org/hco/19/GRCh38#29702517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#37894561-C-A

29702517-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: 37894561-C-G

29702517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: 37894561-C-T

http://identifiers.org/hco/19/GRCh38#29702530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#37894548-C-A

29702530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: 37894548-C-T

http://identifiers.org/hco/19/GRCh38#29702534-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#37894544-A-C

29702534-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: 37894544-A-T

29702551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: 37894527-A-G

29702559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: 37894518-G-T

29702596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: 37894501-C-T

29702600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: 37894497-T-C

29702600-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: 37894497-T-G

http://identifiers.org/hco/19/GRCh38#29702646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#37894459-C-A

http://identifiers.org/hco/19/GRCh38#29702694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#37894410-C-A

http://identifiers.org/hco/19/GRCh38#29702700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#37894404-C-A

29702700-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: 37894404-C-G

29702700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: 37894404-C-T

29702703-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: 37894401-A-T

29702704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: 37894400-G-A

http://identifiers.org/hco/19/GRCh38#29702708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#37894396-C-A

29702708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3 prime UTR variant
orthologous variants: 37894396-C-T

http://identifiers.org/hco/19/GRCh38#29702724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#37894380-C-A

http://identifiers.org/hco/19/GRCh38#29702730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#37894374-C-A

29702730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 37894374-C-T

29702743-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 37894361-T-A

29702767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: missense variant
orthologous variants: 37894337-A-G

29702844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 37894260-G-A

29702844-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 37894260-G-C

29702844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 37894260-G-T

http://identifiers.org/hco/19/GRCh38#29702847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#37894257-C-A

29702847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, splice_donor_variant, synonymous_variant
orthologous variants: 37894257-C-T

http://identifiers.org/hco/19/GRCh38#29702861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#37894243-C-A

29702861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 37894243-C-T

29702865-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 37894239-T-A

29702879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 37894225-T-C

29702883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 37894221-T-C

http://identifiers.org/hco/19/GRCh38#29702961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#37894143-C-A

29702961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 37894143-C-T

29702968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 37894136-A-G

29702969-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 37894135-C-G

29702988-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37894116-T-A

29703044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37894064-A-G

29703047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37894061-G-A

http://identifiers.org/hco/19/GRCh38#29703098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#37894023-C-A

29703098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37894023-C-T

29703101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37894020-G-A

29703101-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37894020-G-T

29703215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37893918-C-T

29703339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37893806-G-A

29703339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37893806-G-T

29704956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37892719-C-T

29705127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37892547-A-G

29705128-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37892546-T-A

29705128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37892546-T-C

29705128-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37892546-T-G

http://identifiers.org/hco/19/GRCh38#29705132-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#37892543-A-C

29705132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37892543-A-G

29705135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37892540-A-G

29705136-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37892539-T-G

29705141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37892534-C-T

http://identifiers.org/hco/19/GRCh38#29705147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#37892528-C-A

29705166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37892520-G-A

29705166-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37892520-G-C

29705166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37892520-G-T

29705170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37892516-G-A

http://identifiers.org/hco/19/GRCh38#29705279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#37892433-C-A

29705279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37892433-C-T

http://identifiers.org/hco/19/GRCh38#29705286-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#37892426-C-A

29705286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37892426-C-T

29705297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37892411-T-C

http://identifiers.org/hco/19/GRCh38#29705333-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#37892373-A-C

29705355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 37892350-A-G

29705355-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 37892350-A-T

29705362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 37892343-G-A

29705362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 37892343-G-T

29706146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37889654-C-T

29706223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37889589-A-G

29706283-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37889533-T-G

29706411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37889402-C-T

29706582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37889250-G-A

http://identifiers.org/hco/19/GRCh38#29706624-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#37889214-A-C

29706662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37889192-C-T

29706808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37889084-C-T

29706837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37889050-C-T

29708114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37888316-G-A

29708147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37888290-G-A

29708147-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37888290-G-C

29708147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37888290-G-T

29708150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37888287-A-G

29708156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37888281-G-T

29708390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 37888063-G-A

29708512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37887592-A-G

http://identifiers.org/hco/19/GRCh38#29708531-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#37887573-A-C

http://identifiers.org/hco/19/GRCh38#29708546-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#37887558-A-C

29708573-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37887534-G-C

29708573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37887534-G-T

http://identifiers.org/hco/19/GRCh38#29708625-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#37887480-A-C

http://identifiers.org/hco/19/GRCh38#29708635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#37887470-C-A

29708637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37887468-G-T

29708654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37887451-T-C

29708657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37887448-T-C

29708695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 37887410-G-A

29708696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 37887409-A-G

29708701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 37887404-C-T

29708711-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 37887393-T-A

29708711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 37887393-T-C

http://identifiers.org/hco/19/GRCh38#29708718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#37887386-C-A

29708723-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 37887381-T-A

29708741-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 37887367-T-A

29708741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 37887367-T-C

29708783-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 37887326-A-T

29708827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 37887265-G-A

29708847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37887244-C-T

29708861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37887233-G-A

29711563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37885489-C-T

29711637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37885423-C-T

29713125-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37884594-G-C

http://identifiers.org/hco/19/GRCh38#29713264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#37884491-C-A

29713306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 37884452-C-T

29713322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37884436-G-A

29713326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37884432-C-T

29713349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37884409-G-A

29713401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37884351-C-T

29713407-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37884335-C-G

http://identifiers.org/hco/19/GRCh38#29714567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#37883608-C-A

29714567-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37883608-C-G

29714601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37883574-A-G

http://identifiers.org/hco/19/GRCh38#29715202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#37883282-C-A

29715202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37883282-C-T

http://identifiers.org/hco/19/GRCh38#29715279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#37883217-C-A

29715279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 37883217-C-T

29715285-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 37883211-C-G

29715285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 37883211-C-T

29715302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 37883195-T-C

29715302-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 37883195-T-G

http://identifiers.org/hco/19/GRCh38#29715324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#37883167-C-A

29715324-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 37883167-C-G

29715324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 37883167-C-T

http://identifiers.org/hco/19/GRCh38#29715330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#37883161-C-A

29715330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 37883161-C-T

29715339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 37883152-A-G

http://identifiers.org/hco/19/GRCh38#29715348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#37883143-C-A

29715348-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 37883143-C-G

29715348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 37883143-C-T

29715388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 37883102-T-C

29715388-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 37883102-T-G

http://identifiers.org/hco/19/GRCh38#29715402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#37883091-C-A

29715402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 37883091-C-T

29715461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: intron_variant, undefined
orthologous variants: 37883032-G-A

http://identifiers.org/hco/19/GRCh38#29715515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#37882990-C-A

29715515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: intron_variant, undefined
orthologous variants: 37882990-C-T

http://identifiers.org/hco/19/GRCh38#29715518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#37882987-C-A

29715518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: intron_variant, undefined
orthologous variants: 37882987-C-T

29715565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, splice_region_variant, undefined
orthologous variants: 37882946-G-A

29715581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 37882930-G-A

29715581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 37882930-G-T

29715646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 37882840-G-T

http://identifiers.org/hco/19/GRCh38#29715654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#37882832-C-A

29715654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 37882832-C-T

29715664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 37882824-T-C

29715669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25443
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 37882819-A-G