http://identifiers.org/hco/2/GRCh38#227614118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#82932849-C-A

227614203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82932942-G-T

227614292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82933034-C-T

227614311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82933052-C-T

227614381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82933118-C-T

227614403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82933138-A-G

227614440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82933170-C-T

227614441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82933171-A-G

http://identifiers.org/hco/2/GRCh38#227614445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#82933175-C-A

227614445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82933175-C-T

227614482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82933220-G-A

227614482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82933220-G-T

227614485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82933223-A-G

227614512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82933286-C-T

227614552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82933326-G-A

http://identifiers.org/hco/2/GRCh38#227614571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#82933342-C-A

http://identifiers.org/hco/2/GRCh38#227614580-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#82933351-A-C

227614580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82933351-A-G

227614610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82933402-G-A

227614610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82933402-G-T

http://identifiers.org/hco/2/GRCh38#227614611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#82933403-C-A

227614611-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82933403-C-G

227614611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82933403-C-T

227614613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82933405-G-A

227614613-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82933405-G-C

227614613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82933405-G-T

227614621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82933413-G-A

227614621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82933413-G-T

227614624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82933416-G-A

227614624-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82933416-G-C

227614624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82933416-G-T

http://identifiers.org/hco/2/GRCh38#227614637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#82933435-C-A

227614637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82933435-C-T

http://identifiers.org/hco/2/GRCh38#227614638-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#82933436-A-C

227614638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82933436-A-G

http://identifiers.org/hco/2/GRCh38#227614639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#82933437-C-A

227614639-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82933437-C-G

227614639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82933437-C-T

227614640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82933438-A-G

227614640-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82933438-A-T

227614664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82933465-G-A

227614676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82933477-G-A

227614682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82933483-G-A

227614682-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82933483-G-C

http://identifiers.org/hco/2/GRCh38#227614705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#82933515-C-A

227614705-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82933515-C-G

227614705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82933515-C-T

http://identifiers.org/hco/2/GRCh38#227614707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#82933517-C-A

227614707-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82933517-C-G

227614707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82933517-C-T

227614709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82933519-G-A

227614709-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82933519-G-C

227614709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82933519-G-T

227614721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82933531-G-A

227614721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82933531-G-T

http://identifiers.org/hco/2/GRCh38#227614745-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#82933558-A-C

227614745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82933558-A-G

227614748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82933561-A-G

227614760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82933576-G-A

227614760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82933576-G-T

http://identifiers.org/hco/2/GRCh38#227614780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#82933602-C-A

227614780-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82933602-C-G

227614780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82933602-C-T

227614781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82933603-A-G

http://identifiers.org/hco/2/GRCh38#227614783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#82933605-C-A

227614783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82933605-C-T

227614784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82933606-G-A

227614784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82933606-G-T

227614811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82933639-A-G

227614814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82933642-A-G

227614819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82933647-T-C

227614820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82933648-T-C

227614823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82933651-A-G

227614823-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82933651-A-T

227614842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82933670-G-A

227614842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82933670-G-T

227614858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82933686-T-C

http://identifiers.org/hco/2/GRCh38#227614885-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#82933712-A-C

227614885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82933712-A-G

227614923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82933750-G-A

227614923-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82933750-G-C

http://identifiers.org/hco/2/GRCh38#227614939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#82933766-C-A

227614958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82933786-G-A

227614958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82933786-G-T

227614983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82933809-T-C

227614989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82933815-T-C

227615000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82933826-G-A

227615135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82933957-G-A

227615316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82934127-G-A

227615467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82934268-C-T

227615475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82934276-C-T

227616280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82936830-G-A

227616451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82936977-C-T

227616454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82936980-G-A

227616454-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82936980-G-C

227616602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82937111-C-T

227616603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82937112-G-A

227616901-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82937410-C-G

227616967-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82937481-T-A

227616967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82937481-T-C

227617101-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82937619-G-T

227617167-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82937677-T-G

227617315-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82937824-C-G

227617315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82937824-C-T

http://identifiers.org/hco/2/GRCh38#227617343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#82937851-C-A

227617365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82937873-G-A

227617401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82937909-G-T

227617406-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82937914-A-T

227617422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82937930-G-A

227617422-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82937930-G-C

227617422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82937930-G-T

227617424-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82937932-A-T

http://identifiers.org/hco/2/GRCh38#227617449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#82937957-C-A

227617449-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82937957-C-G

227617458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82937966-G-A

227617458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82937966-G-T

227617479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 82937986-T-C

227617479-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 82937986-T-G

227617527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82938033-T-C

227617533-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82938039-T-A

227617533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82938039-T-C

227617537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82938043-G-A

227617537-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82938043-G-C

227617537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82938043-G-T

227617551-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82938060-T-A

227617551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82938060-T-C

227617558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82938067-G-A

227617558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82938067-G-T

227617563-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82938075-T-A

227617563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82938075-T-C

227617575-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82938087-T-A

227617575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82938087-T-C

227617582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82938094-G-A

227617582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82938094-G-T

227617591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82938106-T-C

227617591-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82938106-T-G

227617592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82938107-G-A

227617592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82938107-G-T

227617597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82938112-G-A

227617600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82938115-G-A

227617600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82938115-G-T

227617611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82938150-T-C

http://identifiers.org/hco/2/GRCh38#227617626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#82938165-C-A

227617626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82938165-C-T

http://identifiers.org/hco/2/GRCh38#227617635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#82938174-C-A

227617635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82938174-C-T

227617657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82938223-T-C

http://identifiers.org/hco/2/GRCh38#227617659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#82938225-C-A

227617686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82938318-C-T

227617692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82938324-T-C

http://identifiers.org/hco/2/GRCh38#227617725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#82938363-C-A

227617725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82938363-C-T

227617779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82938441-A-G

http://identifiers.org/hco/2/GRCh38#227617821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#82938483-C-A

227617821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82938483-C-T

http://identifiers.org/hco/2/GRCh38#227617904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#82938541-C-A

227617904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82938541-C-T

227617942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82938579-G-A

227617942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82938579-G-T

227618037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82938676-T-C

227618071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82938703-C-T

227618286-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82938910-T-G

http://identifiers.org/hco/2/GRCh38#227618320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#82938935-C-A

http://identifiers.org/hco/2/GRCh38#227618360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#82920175-C-A

227618360-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82920175-C-G

227618360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82920175-C-T

227618378-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82920158-T-G

227618414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82920122-A-G

http://identifiers.org/hco/2/GRCh38#227618415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#82920121-C-A

http://identifiers.org/hco/2/GRCh38#227618416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#82920120-C-A

227618438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82920098-T-C

227618804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82939072-G-T

227618815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82939093-T-C

227629400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82944026-A-G

227629436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82944060-C-T

227629606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82944219-T-C

227629694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82944299-G-A

227629756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82944327-G-A

227630081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82944591-T-C

227630202-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82944702-A-T

227630351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82944928-T-C

227630415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82944993-G-A

227630422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82945000-C-T

http://identifiers.org/hco/2/GRCh38#227630531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#82945094-C-A

227630537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82945100-G-A

227630538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82945101-A-G

227631824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82946996-T-C

227631825-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82946997-A-T

227632613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82947873-G-A

227632613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82947873-G-T

227632708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82947966-G-A

227632726-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82947983-A-T

227632932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82948230-T-C

http://identifiers.org/hco/2/GRCh38#227632941-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#82948249-A-C

227632941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82948249-A-G

227632943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82948251-G-A

227632943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82948251-G-T

227632961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 82948268-G-A

227632961-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 82948268-G-T

227633114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 82992569-T-C

http://identifiers.org/hco/2/GRCh38#227641856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#82948854-C-A

227641951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82948962-G-T

227642044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82949049-A-G

227642144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82949142-A-G

227642169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82949163-T-C

227642170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82949164-G-A

http://identifiers.org/hco/2/GRCh38#227642190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#82949189-C-A

http://identifiers.org/hco/2/GRCh38#227642241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#82949236-C-A

227642241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: non coding transcript exon variant
orthologous variants: 82949236-C-T

227642293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82949291-A-G

227642434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82949505-G-T

227642520-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82949599-C-G

227642637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82949716-A-G

227642796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82949866-A-G

227642805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82949873-C-T

227642965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82950024-G-A

http://identifiers.org/hco/2/GRCh38#227643117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#82950159-C-A

227644425-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82951871-C-G

http://identifiers.org/hco/2/GRCh38#227644495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#82951959-C-A

227648016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: non coding transcript exon variant
orthologous variants: 83000278-T-C

227648017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: non coding transcript exon variant
orthologous variants: 83000279-G-A

227648017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: non coding transcript exon variant
orthologous variants: 83000279-G-T

227648041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: non coding transcript exon variant
orthologous variants: 83000304-G-T

227648088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: non coding transcript exon variant
orthologous variants: 83000345-T-C

227648103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: non coding transcript exon variant
orthologous variants: 83000360-A-G

http://identifiers.org/hco/2/GRCh38#227648110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#83000367-C-A

227648110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: non coding transcript exon variant
orthologous variants: 83000367-C-T

227648147-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: non coding transcript exon variant
orthologous variants: 83000404-G-C

227648147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: non coding transcript exon variant
orthologous variants: 83000404-G-T

http://identifiers.org/hco/2/GRCh38#227648155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#83000412-C-A

227648155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: non coding transcript exon variant
orthologous variants: 83000412-C-T

http://identifiers.org/hco/2/GRCh38#227648295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#83000551-C-A

227648370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: non coding transcript exon variant
orthologous variants: 83000626-G-A

227648370-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: non coding transcript exon variant
orthologous variants: 83000626-G-C

227648384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: non coding transcript exon variant
orthologous variants: 83000640-C-T

227648556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: non coding transcript exon variant
orthologous variants: 83000809-C-T

227648595-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: non coding transcript exon variant
orthologous variants: 83000848-G-C

227648595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25344
most severe consequence: non coding transcript exon variant
orthologous variants: 83000848-G-T