http://identifiers.org/hco/1/GRCh38#200969438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136105688-C-A

200969642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3 prime UTR variant
orthologous variants: 136105469-A-G

http://identifiers.org/hco/1/GRCh38#200969688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136105435-C-A

200969688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3 prime UTR variant
orthologous variants: 136105435-C-T

200969724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3 prime UTR variant
orthologous variants: 136105406-A-G

200969823-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3 prime UTR variant
orthologous variants: 136105294-T-A

200969823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3 prime UTR variant
orthologous variants: 136105294-T-C

200969850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3 prime UTR variant
orthologous variants: 136105271-G-A

200969850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3 prime UTR variant
orthologous variants: 136105271-G-T

200969977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 136105151-A-G

http://identifiers.org/hco/1/GRCh38#200969985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#136105143-C-A

200969985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 136105143-C-T

200970129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3 prime UTR variant
orthologous variants: 136105017-G-T

200970254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 136104899-G-T

http://identifiers.org/hco/1/GRCh38#200970299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#136104858-C-A

200970299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 136104858-C-T

http://identifiers.org/hco/1/GRCh38#200970321-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#136104837-C-A

200970321-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 136104837-C-G

200970321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 136104837-C-T

200970464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 136104718-T-C

200970520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3 prime UTR variant
orthologous variants: 136104657-A-G

200970520-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3 prime UTR variant
orthologous variants: 136104657-A-T

200970535-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3 prime UTR variant
orthologous variants: 136104646-T-A

200970535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3 prime UTR variant
orthologous variants: 136104646-T-C

http://identifiers.org/hco/1/GRCh38#200970536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136104645-C-A

200970536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3 prime UTR variant
orthologous variants: 136104645-C-T

200970589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3 prime UTR variant
orthologous variants: 136104594-G-A

200970589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3 prime UTR variant
orthologous variants: 136104594-G-T

200970654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3 prime UTR variant
orthologous variants: 136104530-T-C

200970678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3 prime UTR variant
orthologous variants: 136104513-T-C

200970692-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3 prime UTR variant
orthologous variants: 136104498-G-C

http://identifiers.org/hco/1/GRCh38#200970790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136104400-C-A

200970790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3 prime UTR variant
orthologous variants: 136104400-C-T

200970875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3 prime UTR variant
orthologous variants: 136104339-G-T

200970971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3 prime UTR variant
orthologous variants: 136104257-A-G

http://identifiers.org/hco/1/GRCh38#200970972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136104256-C-A

200970972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3 prime UTR variant
orthologous variants: 136104256-C-T

http://identifiers.org/hco/1/GRCh38#200970981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136104247-C-A

200970981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3 prime UTR variant
orthologous variants: 136104247-C-T

200970997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3 prime UTR variant
orthologous variants: 136104231-G-T

http://identifiers.org/hco/1/GRCh38#200971020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136104208-C-A

http://identifiers.org/hco/1/GRCh38#200971163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136104063-C-A

200971216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3 prime UTR variant
orthologous variants: 136104006-T-C

200971337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3 prime UTR variant
orthologous variants: 136103898-G-A

200971337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3 prime UTR variant
orthologous variants: 136103898-G-T

200971428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3 prime UTR variant
orthologous variants: 136103795-G-T

http://identifiers.org/hco/1/GRCh38#200971690-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136103542-A-C

200971696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3 prime UTR variant
orthologous variants: 136103536-G-A

200971696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3 prime UTR variant
orthologous variants: 136103536-G-T

200971794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3 prime UTR variant
orthologous variants: 136103433-G-T

200971803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 136103424-G-T

200971897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3 prime UTR variant
orthologous variants: 136103348-G-A

200971897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3 prime UTR variant
orthologous variants: 136103348-G-T

200971956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3 prime UTR variant
orthologous variants: 136103296-G-T

200971957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3 prime UTR variant
orthologous variants: 136103295-C-T

200972039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 136103218-A-G

200972044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 136103213-G-A

200972079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 136103179-G-T

200972145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 136103114-G-A

200972145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 136103114-G-T

200972156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 136103104-T-C

200972242-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 136103024-G-T

200972298-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3 prime UTR variant
orthologous variants: 136102976-G-C

http://identifiers.org/hco/1/GRCh38#200972324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136102950-C-A

200972324-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3 prime UTR variant
orthologous variants: 136102950-C-G

200972324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3 prime UTR variant
orthologous variants: 136102950-C-T

200972352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3 prime UTR variant
orthologous variants: 136102916-G-T

200972475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3 prime UTR variant
orthologous variants: 136102839-G-A

200972475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3 prime UTR variant
orthologous variants: 136102839-G-T

200972481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3 prime UTR variant
orthologous variants: 136102832-G-T

http://identifiers.org/hco/1/GRCh38#200972494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136102819-C-A

200972494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3 prime UTR variant
orthologous variants: 136102819-C-T

200972624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3 prime UTR variant
orthologous variants: 136102694-G-A

200972625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3 prime UTR variant
orthologous variants: 136102693-G-A

http://identifiers.org/hco/1/GRCh38#200972784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136102538-C-A

http://identifiers.org/hco/1/GRCh38#200973260-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136102077-A-C

200973260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3 prime UTR variant
orthologous variants: 136102077-A-G

200973271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3 prime UTR variant
orthologous variants: 136102052-T-C

200973271-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3 prime UTR variant
orthologous variants: 136102052-T-G

200973280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3 prime UTR variant
orthologous variants: 136102043-T-C

200973305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3 prime UTR variant
orthologous variants: 136102018-C-T

200973310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3 prime UTR variant
orthologous variants: 136102013-C-T

200973420-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3 prime UTR variant
orthologous variants: 136101935-T-A

200973420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3 prime UTR variant
orthologous variants: 136101935-T-C

200973441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3 prime UTR variant
orthologous variants: 136101914-T-C

200973445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3 prime UTR variant
orthologous variants: 136101904-C-T

200973580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3_prime_UTR_variant, splice_acceptor_variant
orthologous variants: 136101771-T-C

200973664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 136101687-G-A

200973664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 136101687-G-T

200973701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 136101653-G-A

http://identifiers.org/hco/1/GRCh38#200973707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136101647-C-A

200973707-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 136101647-C-G

200973725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 136101628-G-A

200973725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 136101628-G-T

200973748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 136101605-G-A

200973748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 136101605-G-T

200973773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 136101578-A-G

200974200-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 136101202-T-G

http://identifiers.org/hco/1/GRCh38#200974212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136101179-C-A

200974212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136101179-C-T

200974421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136100988-C-T

200974422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136100987-G-A

200974422-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136100987-G-C

200974429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136100980-G-T

http://identifiers.org/hco/1/GRCh38#200974568-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136100859-A-C

200974619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136100822-G-A

200974619-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136100822-G-C

200974619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136100822-G-T

200974627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136100814-T-C

200974627-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136100814-T-G

200974839-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: synonymous variant
orthologous variants: 136100613-G-C

http://identifiers.org/hco/1/GRCh38#200974971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136100489-C-A

200975001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136100441-A-G

http://identifiers.org/hco/1/GRCh38#200975012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136100430-C-A

200975012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136100430-C-T

200975029-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136100419-T-A

200975029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136100419-T-C

http://identifiers.org/hco/1/GRCh38#200975040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136100408-C-A

200975040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136100408-C-T

200975041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136100407-G-A

200975041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136100407-G-T

200975338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136100170-G-A

200975401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136100128-G-A

200975401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136100128-G-T

200975590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: missense variant
orthologous variants: 136099974-T-C

200975611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: missense variant
orthologous variants: 136099953-G-A

200975644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: missense variant
orthologous variants: 136099920-G-A

200976489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136099690-A-G

200976564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136099630-C-T

http://identifiers.org/hco/1/GRCh38#200976626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136099585-C-A

200976626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136099585-C-T

200976629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136099582-A-G

200976649-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136099564-G-C

200976649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136099564-G-T

200976662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136099551-A-G

200976662-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136099551-A-T

http://identifiers.org/hco/1/GRCh38#200976673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136099540-C-A

200976673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136099540-C-T

http://identifiers.org/hco/1/GRCh38#200976693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136099520-C-A

200976693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136099520-C-T

http://identifiers.org/hco/1/GRCh38#200976704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136099512-C-A

200976704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136099512-C-T

200976724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136099490-G-T

200976739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136099475-A-G

200976741-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136099473-G-T

200976899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 136099318-G-A

http://identifiers.org/hco/1/GRCh38#200976965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136099243-C-A

200976965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136099243-C-T

200976976-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136099232-T-A

200976976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136099232-T-C

200977005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136099203-T-C

http://identifiers.org/hco/1/GRCh38#200977006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136099202-C-A

200977095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136099145-G-A

200977095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136099145-G-T

200977171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136099069-G-A

200977199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136099055-G-A

200977199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136099055-G-T

200977200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136099054-T-C

200977206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136099048-G-A

200977206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136099048-G-T

200977329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: missense variant
orthologous variants: 136098925-G-A

200977428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136098824-G-A

200977428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136098824-G-T

http://identifiers.org/hco/1/GRCh38#200977444-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136098808-A-C

200977446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136098806-A-G

http://identifiers.org/hco/1/GRCh38#200977451-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136098801-A-C

http://identifiers.org/hco/1/GRCh38#200977470-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136098782-A-C

200977501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136098753-G-A

200977501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136098753-G-T

200977506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136098748-A-G

200977511-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136098743-A-T

http://identifiers.org/hco/1/GRCh38#200977526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136098731-C-A

200977526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136098731-C-T

200977582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136098685-T-C

200977591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136098676-C-T

200977675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136098589-C-T

200979405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136098004-G-T

200979414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136097997-T-C

http://identifiers.org/hco/1/GRCh38#200979427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136097984-C-A

200979427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136097984-C-T

200979451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136097960-G-A

200979451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136097960-G-T

http://identifiers.org/hco/1/GRCh38#200979507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136097930-C-A

200979507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136097930-C-T

200979521-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136097916-C-G

200979521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136097916-C-T

200979649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: missense_variant, undefined
orthologous variants: 136097791-T-C

http://identifiers.org/hco/1/GRCh38#200979682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136097758-C-A

200979682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: missense variant
orthologous variants: 136097758-C-T

200979722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 136097718-G-T

200979863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, undefined
orthologous variants: 136097686-A-G

200979863-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, undefined
orthologous variants: 136097686-A-T

200980598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136097330-G-A

http://identifiers.org/hco/1/GRCh38#200980924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136097094-C-A

200980924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136097094-C-T

http://identifiers.org/hco/1/GRCh38#200980931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136097087-C-A

200980944-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136097070-T-A

200980944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136097070-T-C

200980945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136097069-T-C

200981036-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: synonymous variant
orthologous variants: 136096983-G-C

200981060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: synonymous variant
orthologous variants: 136096959-T-C

200981060-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: synonymous variant
orthologous variants: 136096959-T-G

200981067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: missense variant
orthologous variants: 136096952-T-C

200981079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: missense variant
orthologous variants: 136096940-A-G

200981107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136096912-G-A

200981107-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136096912-G-C

200981191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136096836-G-A

200981200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136096827-G-A

200981200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136096827-G-T

200981325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136096743-C-T

200981357-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136096717-C-G

http://identifiers.org/hco/1/GRCh38#200981672-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136096445-A-C

200981804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136096136-C-T

200981805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136096135-C-T

200981857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136096083-C-T

200981950-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136096018-G-C

200982739-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136095274-T-A

200982937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136095053-G-A

200982937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136095053-G-T

200982938-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136095052-G-C

200982938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136095052-G-T

200982950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136095040-G-A

200982950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136095040-G-T

http://identifiers.org/hco/1/GRCh38#200982958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136095032-C-A

200982958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136095032-C-T

200983015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136094977-T-C

200983015-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136094977-T-G

200983025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136094967-G-A

200983025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136094967-G-T

200983154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136094839-G-A

200983154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136094839-G-T

http://identifiers.org/hco/1/GRCh38#200983238-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136094752-C-A

200983238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136094752-C-T

200983261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136094728-G-A

200983455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136094528-G-A

200983487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136094496-G-A

200983679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136094185-A-G

200984204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136093561-C-T

200984361-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136093404-C-G

200984361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136093404-C-T

200984406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136093360-G-A

200984535-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136093165-G-C

200984743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136092962-G-A

200984743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136092962-G-T

http://identifiers.org/hco/1/GRCh38#200984778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136092930-C-A

200984778-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136092930-C-G

200984778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136092930-C-T

200984799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136092925-C-T

200984833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136092893-C-T

200984838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136092888-T-C

200984865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: missense variant
orthologous variants: 136092861-A-G

200984865-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: missense variant
orthologous variants: 136092861-A-T

200984895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: missense variant
orthologous variants: 136092831-A-G

200985016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136092710-G-A

http://identifiers.org/hco/1/GRCh38#200985028-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136092700-C-A

200985028-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136092700-C-G

200985028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136092700-C-T

http://identifiers.org/hco/1/GRCh38#200985075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136092662-C-A

200985075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136092662-C-T

200985100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136092636-G-A

200985559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136091396-C-T

200985608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136091346-G-A

200986193-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136091209-T-G

200986258-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136091146-T-A

200986666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136091051-C-T

200986683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136091034-G-A

200986683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136091034-G-T

200986716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136091003-G-A

200986716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136091003-G-T

http://identifiers.org/hco/1/GRCh38#200986717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136091002-C-A

200986717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136091002-C-T

200986836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 136090894-G-A

200986880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: missense variant
orthologous variants: 136090850-G-A

200986880-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: missense variant
orthologous variants: 136090850-G-C

200986886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: missense variant
orthologous variants: 136090844-G-A

200986933-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136090794-T-A

200987258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136090469-G-A

200987258-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136090469-G-C

200987265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136090462-G-T

200987266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136090461-G-A

200987266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136090461-G-T

200987694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136090299-T-C

200987726-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136090268-C-G

200987874-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136090140-G-C

http://identifiers.org/hco/1/GRCh38#200988082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136089975-C-A

200988185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136089861-G-A

200988185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136089861-G-T

200988233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136089817-G-A

200988336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: missense variant
orthologous variants: 136089717-G-A

200988336-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: missense variant
orthologous variants: 136089717-G-T

200988417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136089592-G-A

http://identifiers.org/hco/1/GRCh38#200988591-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136089418-A-C

200988591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136089418-A-G

200988804-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: missense variant
orthologous variants: 136089269-T-G

http://identifiers.org/hco/1/GRCh38#200988966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136089107-C-A

200988966-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136089107-C-G

200988966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136089107-C-T

200989255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136088745-G-A

200989644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136088392-T-C

200989771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136088296-G-A

200989801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136088265-A-G

200989837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136088229-G-A

200989837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136088229-G-T

200989838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136088228-T-C

200990018-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: missense variant
orthologous variants: 136088065-G-C

http://identifiers.org/hco/1/GRCh38#200990046-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136088033-A-C

http://identifiers.org/hco/1/GRCh38#200990049-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136088030-A-C

200990049-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 136088030-A-T

200990082-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136087998-A-T

200990109-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136087972-C-G

200990109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136087972-C-T

http://identifiers.org/hco/1/GRCh38#200990370-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136087712-A-C

200990428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136087651-A-G

http://identifiers.org/hco/1/GRCh38#200990452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136087637-C-A

200990452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136087637-C-T

200990460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136087629-G-A

200990460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136087629-G-T

200990520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136087575-G-T

200990716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: missense variant
orthologous variants: 136087381-A-G

200990789-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136087304-C-G

200990823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136087273-A-G

200990844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136087257-C-T

http://identifiers.org/hco/1/GRCh38#200990845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136087256-C-A

200990845-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136087256-C-G

200991184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136086941-G-A

200991595-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136086171-A-T

200991625-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136086130-C-G

200991625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136086130-C-T

200991734-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136086014-G-C

http://identifiers.org/hco/1/GRCh38#200991803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136085758-C-A

200991803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136085758-C-T

http://identifiers.org/hco/1/GRCh38#200991841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136085712-C-A

200991841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136085712-C-T

200991860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136085693-G-T

200991876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136085677-A-G

200992030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136085532-T-C

200992143-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136085420-C-G

200992143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136085420-C-T

200992206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136085370-G-A

200992206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136085370-G-T

http://identifiers.org/hco/1/GRCh38#200992223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136085355-C-A

200992223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136085355-C-T

200992229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136085349-G-A

200992229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136085349-G-T

200992239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136085339-C-T

200992242-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136085336-G-T

200992248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136085328-A-G

200992432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136085157-G-A

200992432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136085157-G-T

200994932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136084978-G-A

200995079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136084864-C-T

http://identifiers.org/hco/1/GRCh38#200995164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136084823-C-A

200995251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136084739-T-C

200995367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136084655-G-A

http://identifiers.org/hco/1/GRCh38#200996182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136084044-C-A

200996230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: missense variant
orthologous variants: 136083998-A-G

200996230-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: missense variant
orthologous variants: 136083998-A-T

200996284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: missense variant
orthologous variants: 136083944-T-C

200996329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: missense variant
orthologous variants: 136083899-C-T

200996347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: missense variant
orthologous variants: 136083881-T-C

200996347-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: missense variant
orthologous variants: 136083881-T-G

200996397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: splice acceptor variant
orthologous variants: 136083831-T-C

http://identifiers.org/hco/1/GRCh38#200996431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136083802-C-A

200996431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136083802-C-T

200996469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136083768-G-A

200996469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136083768-G-T

200996750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136083597-G-A

200997046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136083360-C-T

200998416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: missense variant
orthologous variants: 136081999-T-C

200998473-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: missense variant
orthologous variants: 136081942-A-T

200998557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: missense variant
orthologous variants: 136081858-T-C

200998579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 136081836-T-C

http://identifiers.org/hco/1/GRCh38#200998675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136081738-C-A

200998675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136081738-C-T

200998772-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136081658-G-C

200998800-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136081630-C-G

200999326-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136081068-G-C

http://identifiers.org/hco/1/GRCh38#200999420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136080975-C-A

200999420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: missense variant
orthologous variants: 136080975-C-T

200999494-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 136080898-C-G

200999494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, splice_region_variant, synonymous_variant
orthologous variants: 136080898-C-T

http://identifiers.org/hco/1/GRCh38#200999495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, splice_acceptor_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136080897-C-A

http://identifiers.org/hco/1/GRCh38#200999516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136080876-C-A

200999544-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136080848-G-C

200999544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136080848-G-T

200999575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136080835-G-A

200999575-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136080835-G-C

200999753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136080680-A-G

200999831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136080615-G-A

200999831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136080615-G-T

http://identifiers.org/hco/1/GRCh38#200999832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136080614-C-A

200999836-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136080610-G-C

200999836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136080610-G-T

200999850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136080601-A-G

201000129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136080380-A-G

201000171-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136080361-G-C

201000196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136080343-G-A

201000196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136080343-G-T

http://identifiers.org/hco/1/GRCh38#201000255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136080285-C-A

201000255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136080285-C-T

http://identifiers.org/hco/1/GRCh38#201000285-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136080256-A-C

201000285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136080256-A-G

201000307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136080235-G-A

201000307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136080235-G-T

http://identifiers.org/hco/1/GRCh38#201000313-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136080229-C-A

201000313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136080229-C-T

http://identifiers.org/hco/1/GRCh38#201000321-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136080221-C-A

201000321-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136080221-C-G

201000367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136080174-G-A

201000367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136080174-G-T

http://identifiers.org/hco/1/GRCh38#201000369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136080172-C-A

201000369-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136080172-C-G

201000369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136080172-C-T

201000371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136080170-G-A

201000371-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136080170-G-C

http://identifiers.org/hco/1/GRCh38#201000425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136080116-C-A

201000425-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 136080116-C-G

201000425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 136080116-C-T

201000543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: missense variant
orthologous variants: 136079998-G-A

201000792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136079767-C-T

201000808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136079755-G-A

http://identifiers.org/hco/1/GRCh38#201001681-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136079489-A-C

201001713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 136079453-T-C

201001713-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 136079453-T-G

http://identifiers.org/hco/1/GRCh38#201001780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136079386-C-A

201001833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 136079332-A-G

201001852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 136079314-A-G

201001979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 136079203-G-A

201001979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 136079203-G-T

201002006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 136079185-A-G

http://identifiers.org/hco/1/GRCh38#201002078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136079127-C-A

201002078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 136079127-C-T

201002103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 136079103-G-A

201002103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 136079103-G-T

201002145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 136079072-G-A

201002145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 136079072-G-T

201002391-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 136078826-T-G

201002530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 136078703-C-T

201002539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 136078694-T-C

201002555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 136078625-A-G

201002672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 136078457-G-A

201002672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 136078457-G-T

http://identifiers.org/hco/1/GRCh38#201002674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136078455-C-A

http://identifiers.org/hco/1/GRCh38#201002700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136078425-C-A

201002710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 136078415-G-A

201002710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 136078415-G-T

201002765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 136078365-G-T

201002778-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 136078346-T-A

201002778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 136078346-T-C

201002779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 136078345-G-A

201002779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 136078345-G-T

201002849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 136077891-G-A

201002849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 136077891-G-T

http://identifiers.org/hco/1/GRCh38#201002855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136077885-C-A

201002986-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 136077786-T-G

201003067-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 136077699-T-G

http://identifiers.org/hco/1/GRCh38#201003085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_exon_variant, start_lost
orthologous variants: http://identifiers.org/mco/1/GRCm39#136077681-C-A

201003136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 136077630-A-G

201003250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 136077523-A-G

http://identifiers.org/hco/1/GRCh38#201003298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136077474-C-A

201003298-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 136077474-C-G

201003298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 136077474-C-T

http://identifiers.org/hco/1/GRCh38#201003321-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136077451-A-C

201003321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 136077451-A-G

201003327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 136077445-G-A

201003327-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 136077445-G-C

201003347-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 136077427-A-T

http://identifiers.org/hco/1/GRCh38#201003374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136077401-C-A

201003418-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 136077361-G-T

http://identifiers.org/hco/1/GRCh38#201003456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136077327-C-A

201003541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 136077243-C-T

201003577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 136077201-C-T

201003746-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136077032-T-A

201003797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136076981-G-T

201003923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136076867-G-A

201004103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136076699-G-A

201004227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136076577-G-T

http://identifiers.org/hco/1/GRCh38#201004237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136076567-C-A

201004288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136076516-A-G

201004295-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136076509-T-A

201004295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136076509-T-C

201004299-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136076505-T-A

201004299-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136076505-T-G

201004300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136076504-G-T

201004382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136076435-G-A

201004382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136076435-G-T

201004397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136076420-A-G

201004448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136076369-A-G

201004450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 136076367-G-A

201004450-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 136076367-G-T

201004507-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136076317-G-C

201004649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 136076226-A-G

201004728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 136076151-G-A

201004728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 136076151-G-T

201004866-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136076013-G-C

201004895-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 136075981-A-T

201004905-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136075971-T-G

http://identifiers.org/hco/1/GRCh38#201004965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136075911-C-A

201004965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136075911-C-T

http://identifiers.org/hco/1/GRCh38#201005008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136075862-C-A

http://identifiers.org/hco/1/GRCh38#201005051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136075821-C-A

201005051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136075821-C-T

201005190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136075715-A-G

201005190-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136075715-A-T

http://identifiers.org/hco/1/GRCh38#201005212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136075695-C-A

201005212-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136075695-C-G

201005222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136075685-A-G

201005405-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136075507-G-C

201005405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136075507-G-T

201005478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136075434-C-T

http://identifiers.org/hco/1/GRCh38#201005486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136075426-C-A

201005585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136075343-G-A

201005585-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136075343-G-C

201005699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 136075228-G-A

201005699-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 136075228-G-T

201005787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136075158-G-A

201005787-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136075158-G-C

201005787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136075158-G-T

201005886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136075098-G-T

201005929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136075055-G-A

201005979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136075008-G-A

201005979-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136075008-G-C

201005979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136075008-G-T

201006170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136074794-G-T

201006413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136074506-G-A

201006418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136074501-T-C

201006418-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136074501-T-G

201006425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136074496-A-G

201006556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, undefined
orthologous variants: 136074368-G-A

201006562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, undefined
orthologous variants: 136074358-A-G

201006616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136074307-A-G

201006706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136074227-G-A

201006783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136074162-C-T

201006793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136074151-G-T

http://identifiers.org/hco/1/GRCh38#201006812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136074132-C-A

201006812-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136074132-C-G

201006816-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136074128-A-T

201006837-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136074107-G-C

201006841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136074103-C-T

201006851-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136074093-G-C

201006857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136074087-C-T

201006859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136074085-G-A

201006859-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136074085-G-C

201007739-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136074031-C-G

201007808-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136073968-A-T

201008175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136073580-G-A

201008179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136073576-C-T

201008531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136073264-G-T

201008628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136073190-T-C

http://identifiers.org/hco/1/GRCh38#201008679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136073139-C-A

201008679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136073139-C-T

201008697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136073121-A-G

201008738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136073079-C-T

http://identifiers.org/hco/1/GRCh38#201008743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136073074-C-A

201008818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: missense variant
orthologous variants: 136072999-T-C

201008841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: synonymous variant
orthologous variants: 136072976-G-A

201008841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: synonymous variant
orthologous variants: 136072976-G-T

201008896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: missense variant
orthologous variants: 136072921-T-C

201008905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: missense variant
orthologous variants: 136072912-G-A

201008905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: missense variant
orthologous variants: 136072912-G-T

201008983-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136072831-T-G

201009013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136072804-T-C

201009017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136072800-T-C

201009050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136072770-G-A

201009050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136072770-G-T

http://identifiers.org/hco/1/GRCh38#201009189-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136072635-A-C

201009493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 136072330-C-T

201009553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136072272-C-T

http://identifiers.org/hco/1/GRCh38#201009581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136072240-C-A

201009581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136072240-C-T

http://identifiers.org/hco/1/GRCh38#201009585-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136072236-A-C

201009585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136072236-A-G

201009600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136072223-A-G

http://identifiers.org/hco/1/GRCh38#201009619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136072206-C-A

201009619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136072206-C-T

201009967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136071912-G-A

201009967-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136071912-G-C

201010036-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136071839-C-G

201010036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136071839-C-T

201010102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136071779-C-T

201010786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136071170-C-T

201010844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136071113-A-G

201010918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136071062-G-A

http://identifiers.org/hco/1/GRCh38#201011189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136070794-C-A

201011251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136070732-T-C

201011404-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136070577-C-G

201011427-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136070561-C-G

201011454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136070541-C-T

201011457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136070538-A-G

201012089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136069977-G-A

201012089-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136069977-G-T

201012120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136069958-G-A

201012177-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136069915-C-G

201012177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136069915-C-T

201012193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136069899-G-A

201012607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136069566-C-T

201013488-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136069136-C-G

201013736-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136068607-G-T

201013789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136068539-C-T

http://identifiers.org/hco/1/GRCh38#201013807-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136068500-A-C

201014238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, undefined
orthologous variants: 136068154-G-A

201014238-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, undefined
orthologous variants: 136068154-G-C

201014517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, undefined
orthologous variants: 136067935-T-C

201014563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, undefined
orthologous variants: 136067892-G-A

201014563-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, undefined
orthologous variants: 136067892-G-C

201014569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, undefined
orthologous variants: 136067886-G-A

http://identifiers.org/hco/1/GRCh38#201014707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136067753-C-A

201014707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136067753-C-T

201015048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136066883-C-T

201015055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136066876-G-A

201015288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136066697-C-T

201015353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136066630-C-T

201015583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136066381-G-T

201015645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, undefined
orthologous variants: 136066316-C-T

201015849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136066100-G-T

201016039-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, undefined
orthologous variants: 136065946-T-G

201016111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136065879-T-C

201016184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136065800-T-C

http://identifiers.org/hco/1/GRCh38#201016242-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136065732-A-C

201016611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136065339-G-A

201016627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136065323-G-A

201016844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136065124-T-C

201017134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136064862-C-T

201017651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136064341-G-A

201017651-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136064341-G-C

201019225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136063301-G-A

201019389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, undefined
orthologous variants: 136063184-A-G

http://identifiers.org/hco/1/GRCh38#201019426-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136063148-A-C

201019459-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, undefined
orthologous variants: 136063133-G-C

201019571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, undefined
orthologous variants: 136063031-T-C

201019966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136062611-G-T

201020364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron_variant, undefined
orthologous variants: 136062248-G-A

201020568-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136062066-C-G

201020593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136062052-G-A

201021015-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136061728-T-A

201021199-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136061558-T-G

201021316-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136061452-G-C

201021332-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136061440-G-C

201021534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136061288-A-G

http://identifiers.org/hco/1/GRCh38#201021539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136061283-C-A

201021692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136061118-T-C

201021842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136060968-C-T

201021886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136060924-C-T

201021979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136060829-A-G

http://identifiers.org/hco/1/GRCh38#201022034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136060772-C-A

201022111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136060682-T-C

http://identifiers.org/hco/1/GRCh38#201022213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136060596-C-A

http://identifiers.org/hco/1/GRCh38#201022371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136060435-C-A

201022447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136060359-A-G

http://identifiers.org/hco/1/GRCh38#201022711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136060094-C-A

201022711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136060094-C-T

http://identifiers.org/hco/1/GRCh38#201023262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136059578-C-A

201023262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: intron variant
orthologous variants: 136059578-C-T

201023389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 5 prime UTR variant
orthologous variants: 136059452-T-C

http://identifiers.org/hco/1/GRCh38#201023640-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29442
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#136059205-A-C