167630097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 165535804-G-A

167630097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 165535804-G-T

167630253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 165535639-G-A

167630253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 165535639-G-T

167630333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 165535558-G-A

167630333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 165535558-G-T

167630346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 165535545-G-A

167630346-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 165535545-G-C

167630346-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 165535545-G-T

167630392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 165535498-T-C

167630393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 165535497-G-A

167630393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 165535497-G-T

167630406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 165535481-A-G

167630406-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 165535481-A-T

167630449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 165535441-G-A

167630449-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 165535441-G-T

http://identifiers.org/hco/1/GRCh38#167630482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#165535410-C-A

167630482-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 165535410-C-G

167630482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 165535410-C-T

http://identifiers.org/hco/1/GRCh38#167630500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165535393-C-A

167630500-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 165535393-C-G

167630500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 165535393-C-T

167630502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 165535391-G-A

167630502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 165535391-G-T

http://identifiers.org/hco/1/GRCh38#167630537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#165535352-C-A

167630632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 165535302-G-A

167630632-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 165535302-G-T

167630722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165535214-A-G

167630722-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165535214-A-T

167630916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165535042-G-A

http://identifiers.org/hco/1/GRCh38#167630938-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165535024-A-C

167630938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165535024-A-G

167630983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 165534981-T-C

167630986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165534978-T-C

167631051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165534915-G-A

167631805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165534436-G-A

167631805-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165534436-G-C

167632072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165534202-G-A

167632113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165534163-A-G

167632243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165534052-A-G

167632321-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165534003-T-G

167632355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165533971-G-A

167632356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165533970-C-T

167632379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 165533945-T-C

167632379-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 165533945-T-G

167632520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165533803-G-A

167632548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165533780-G-T

167632575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165533747-C-T

167632580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165533743-G-A

167632614-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165533710-T-G

167632656-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165533672-A-T

167632674-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165533653-T-G

http://identifiers.org/hco/1/GRCh38#167632804-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165533548-A-C

167633001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165533370-G-A

167633049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165533322-G-A

167633210-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165533164-T-G

167633520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165532870-G-T

167633718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 165532698-T-C

http://identifiers.org/hco/1/GRCh38#167633804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165532639-C-A

167633804-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 165532639-C-G

http://identifiers.org/hco/1/GRCh38#167633830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165532608-C-A

167633867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165532588-G-T

167634046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165532348-G-A

167634078-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165532317-T-G

167634201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165532256-A-G

http://identifiers.org/hco/1/GRCh38#167634362-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165532132-A-C

http://identifiers.org/hco/1/GRCh38#167634393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165532068-C-A

167634393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165532068-C-T

167634396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165532065-G-A

167634518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165531947-T-C

http://identifiers.org/hco/1/GRCh38#167635592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#165530357-C-A

167635616-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 165530333-G-C

167635761-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165530198-T-A

167635836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165530127-T-C

167635861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165530103-T-C

167635958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165530002-G-A

167636040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165529901-G-A

167636187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165529753-A-G

167636314-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165529657-T-A

167636341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165529641-C-T

167636354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165529628-T-C

167637034-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165529064-T-G

167637035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165529063-G-A

167637035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165529063-G-T

167637431-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 165528700-T-A

167637482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 165528638-G-A

167637482-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 165528638-G-C

167637850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165528324-G-A

167637925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165528250-A-G

167638118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 165528043-C-T

167638246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165527916-G-T

167638282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165527879-G-T

167638291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165527870-C-T

167638292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165527869-A-G

167638334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165527830-T-C

167638433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 165527745-G-T

167638486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165527693-G-A

167639069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165527363-T-C

http://identifiers.org/hco/1/GRCh38#167639140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#165527298-C-A

http://identifiers.org/hco/1/GRCh38#167639146-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165527290-A-C

167639146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165527290-A-G

167639291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165527164-G-A

167639359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165527127-A-G

167639594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165526974-A-G

http://identifiers.org/hco/1/GRCh38#167639694-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165526904-A-C

167639715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165526870-A-G

167639724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165526864-C-T

167639859-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165526749-A-T

167639946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165526670-G-A

167640259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165526435-G-A

http://identifiers.org/hco/1/GRCh38#167640260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165526434-C-A

http://identifiers.org/hco/1/GRCh38#167640266-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165526428-C-A

167640293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165526401-G-A

http://identifiers.org/hco/1/GRCh38#167640304-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165526390-A-C

167640304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165526390-A-G

http://identifiers.org/hco/1/GRCh38#167640320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165526374-C-A

167640425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 165526298-G-A

167640425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 165526298-G-T

http://identifiers.org/hco/1/GRCh38#167640465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165526255-C-A

http://identifiers.org/hco/1/GRCh38#167640485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165526234-C-A

167640530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165526189-G-A

167641840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 165525762-G-A

167641851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 165525751-T-C

167641921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 165525681-A-G

http://identifiers.org/hco/1/GRCh38#167641950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165525650-C-A

167641966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 165525634-G-A

167642136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 165525563-A-G

167642136-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 165525563-A-T

167642140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 165525559-A-G

167642150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 165525549-G-T

167642192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 165525504-A-G

167642745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 165524789-G-A

167642987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 165524604-C-T

167643001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 165524590-C-T

167643043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 165524548-C-T

167643530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165523551-G-A

167643579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165523497-G-A

167643833-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165523273-T-G

167645312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165521518-G-T

167645364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165521459-T-C

167645753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165521256-G-T

167645946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165521102-C-T

167646043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165520984-C-T

167647195-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165520410-T-A

167647225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165520377-G-A

167647253-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165520347-C-G

167648072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165519796-T-C

167648076-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165519792-A-T

167648199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165519674-A-G

http://identifiers.org/hco/1/GRCh38#167648687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165519197-C-A

167648688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165519196-C-T

167648816-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165519094-T-G

167648984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165518918-G-A

167649249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165518702-C-T

167649269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165518699-T-C

167649314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165518656-C-T

167649382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165518608-A-G

167649412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165518579-A-G

167649428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165518563-G-A

167649428-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165518563-G-C

167649436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165518555-C-T

167649506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165518498-C-T

167649625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165518396-G-A

http://identifiers.org/hco/1/GRCh38#167649770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165518258-C-A

http://identifiers.org/hco/1/GRCh38#167649936-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165518124-A-C

167650151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165517925-A-G

http://identifiers.org/hco/1/GRCh38#167650182-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165517894-A-C

167650497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165517610-G-A

167650634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165517508-C-T

167651139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165516417-T-C

167651258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165516296-C-T

167651297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165516250-G-T

http://identifiers.org/hco/1/GRCh38#167651337-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165516210-C-A

167651337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165516210-C-T

167651769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165515877-G-A

167651920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165515663-C-T

167652439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165515456-T-C

167652521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165515376-G-A

167652635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165515256-C-T

167652665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165515218-A-G

167652878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165514997-C-T

167652950-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165514916-T-G

167653321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165514608-G-A

167653409-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165514529-T-G

167653679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165514257-C-T

167654018-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165513883-G-C

167654024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165513877-A-G

167654697-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165512859-G-C

167654750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165512811-G-A

http://identifiers.org/hco/1/GRCh38#167654759-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165512802-A-C

http://identifiers.org/hco/1/GRCh38#167654814-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165512757-A-C

167654814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165512757-A-G

167654858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165512720-A-G

167655017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165512572-G-T

167655103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165512524-G-A

167655206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165512416-A-G

167655264-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165512352-T-G

167655424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165512203-C-T

http://identifiers.org/hco/1/GRCh38#167655523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165512111-C-A

167655536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165512099-G-A

167655536-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165512099-G-C

http://identifiers.org/hco/1/GRCh38#167655555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165512080-C-A

167655568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165512067-A-G

167655594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165512031-T-C

167655598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165512027-C-T

167655789-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165511835-C-G

167655939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165511706-G-A

167656058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165511590-T-C

167656078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165511570-T-C

167656282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165510914-G-A

167656309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165510887-T-C

167656316-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165510880-G-C

167656659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165510617-G-A

167656785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165510508-G-A

167656869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165510427-G-A

167657063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165510274-G-A

167657125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165510215-T-C

167657256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165510095-T-C

167657388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165509977-G-A

167657481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165509917-G-A

167657614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165509798-C-T

167657670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165509742-T-C

167658129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165509451-C-T

167659699-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165507529-T-G

167660009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165507237-A-G

167668482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165506182-A-G

http://identifiers.org/hco/1/GRCh38#167668554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165506113-C-A

167668554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165506113-C-T

167668629-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165506045-C-G

167668688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165505993-G-A

167668780-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165505922-G-C

167669247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165505480-T-C

167669465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165505221-A-G

167669608-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165505083-A-T

167669663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165505030-T-C

167669951-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165504703-T-A

167670047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165504642-C-T

167670178-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165504554-T-G

167670676-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165504132-C-G

167670720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165504089-T-C

167670796-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165504032-T-A

http://identifiers.org/hco/1/GRCh38#167672723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165503253-C-A

167672723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165503253-C-T

167672731-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165503245-T-A

167672781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165503193-C-T

167672875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165503128-A-G

167672888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165503117-C-T

167672971-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165503044-G-C

167673057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165502951-G-T

http://identifiers.org/hco/1/GRCh38#167673195-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165502836-A-C

167673890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165502128-A-G

167673941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165502094-T-C

167673985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165502050-A-G

http://identifiers.org/hco/1/GRCh38#167674021-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165502029-A-C

167674278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165501738-C-T

167676039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165500725-A-G

167676484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165499441-C-T

167676500-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165499425-A-T

http://identifiers.org/hco/1/GRCh38#167676848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165499128-C-A

167676900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165499077-C-T

167676948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165499051-G-A

167676999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165498998-G-A

167677315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165498710-C-T

167678029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165498640-C-T

167678129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165498556-G-A

167678285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165498416-G-A

http://identifiers.org/hco/1/GRCh38#167678436-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165498110-A-C

167678436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165498110-A-G

167678458-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165498083-A-T

167678535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165498001-T-C

167679072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165497492-T-C

167679143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165497452-A-G

167679143-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165497452-A-T

167679160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165497435-T-C

167679271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165497334-T-C

167679385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165497249-T-C

http://identifiers.org/hco/1/GRCh38#167679450-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165497186-A-C

167679472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165497164-C-T

http://identifiers.org/hco/1/GRCh38#167679679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165496959-C-A

167679679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165496959-C-T

167679787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165496823-A-G

167680004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165496608-G-A

167680019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, undefined
orthologous variants: 165496594-G-A

167680323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165496272-T-C

167680327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165496268-C-T

167680399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165496204-C-T

167680466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165496146-T-C

167680979-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165495772-T-G

http://identifiers.org/hco/1/GRCh38#167681080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165495675-C-A

167681080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165495675-C-T

167681198-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165495556-T-G

167681232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165495537-G-A

167681232-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165495537-G-C

167681232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165495537-G-T

167681327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165495479-C-T

167681332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165495474-G-A

167681571-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165495266-C-G

167681941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165494896-C-T

167682051-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165494789-G-C

167683039-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165493634-G-C

167683149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165493557-C-T

167683276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165493451-G-A

167683276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165493451-G-T

167683755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165492758-G-A

167683755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165492758-G-T

167683807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165492709-A-G

167683807-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165492709-A-T

167684037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, undefined
orthologous variants: 165492481-G-T

167684041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, undefined
orthologous variants: 165492477-G-A

167684041-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, undefined
orthologous variants: 165492477-G-C

http://identifiers.org/hco/1/GRCh38#167684042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#165492476-C-A

167684042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, undefined
orthologous variants: 165492476-C-T

167684045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, undefined
orthologous variants: 165492473-G-A

167684045-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, undefined
orthologous variants: 165492473-G-C

167684045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, undefined
orthologous variants: 165492473-G-T

167684200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, undefined
orthologous variants: 165492377-G-T

167684334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165492255-T-C

167684755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165491868-G-T

167684798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165491830-C-T

167684860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165491777-G-A

167685167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165491422-G-A

167685250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165491367-C-T

http://identifiers.org/hco/1/GRCh38#167685379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165491263-C-A

167685379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165491263-C-T

167685421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 165491222-A-G

167685535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165491080-A-G

167685543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165491040-G-A

http://identifiers.org/hco/1/GRCh38#167685590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165491004-C-A

167685590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165491004-C-T

http://identifiers.org/hco/1/GRCh38#167685613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165490980-C-A

http://identifiers.org/hco/1/GRCh38#167685616-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165490977-A-C

167685616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165490977-A-G

167685630-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165490963-A-T

167685632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165490961-T-C

167685641-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165490952-T-G

167685879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165490809-G-A

167686050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165490636-C-T

167686225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165490458-A-G

167686362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165490326-A-G

167686808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165489470-T-C

167686853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165489438-G-T

167686909-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165489388-T-A

167687140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165489185-C-T

167687797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165488786-A-G

167687846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165488754-G-A

167687858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165488743-T-C

167687968-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165488659-C-G

http://identifiers.org/hco/1/GRCh38#167688021-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165488608-A-C

http://identifiers.org/hco/1/GRCh38#167688200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165488425-C-A

167688415-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165488297-G-C

167688453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165488259-C-T

167688458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165488254-A-G

167689022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165487694-G-A

167689517-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165487535-T-A

167689655-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165487390-G-C

http://identifiers.org/hco/1/GRCh38#167689800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165487234-C-A

167689916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165487122-T-C

167689916-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165487122-T-G

167689922-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165487118-A-T

167690022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165487038-G-A

167690022-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165487038-G-C

167690022-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165487038-G-T

167690062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron_variant, missense_variant
orthologous variants: 165486998-A-G

167693049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165486548-A-G

167693231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165486341-G-A

167693644-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165485793-A-T

167693980-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165485362-T-A

167693980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165485362-T-C

167694153-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: missense variant
orthologous variants: 165485215-C-G

167694169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: missense variant
orthologous variants: 165485199-T-C

167694264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: stop gained
orthologous variants: 165485104-C-T

http://identifiers.org/hco/1/GRCh38#167694267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165485101-C-A

167694267-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: missense variant
orthologous variants: 165485101-C-G

167694267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: missense variant
orthologous variants: 165485101-C-T

167694312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165485056-A-G

167697244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: missense variant
orthologous variants: 165483458-T-C

167697244-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: missense variant
orthologous variants: 165483458-T-G

167697379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: missense variant
orthologous variants: 165483317-A-G

http://identifiers.org/hco/1/GRCh38#167697440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165483263-C-A

167697440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: synonymous variant
orthologous variants: 165483263-C-T

167697482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: synonymous variant
orthologous variants: 165483223-G-A

167697510-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: missense variant
orthologous variants: 165483195-T-A

167697510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: missense variant
orthologous variants: 165483195-T-C

167697537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: missense variant
orthologous variants: 165483168-G-T

http://identifiers.org/hco/1/GRCh38#167697593-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165483106-A-C

167697606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: missense variant
orthologous variants: 165483096-G-A

167697627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: stop gained
orthologous variants: 165483075-G-T

167697713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: synonymous variant
orthologous variants: 165482986-G-A

167697713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: missense variant
orthologous variants: 165482986-G-T

http://identifiers.org/hco/1/GRCh38#167697773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165482935-C-A

167697777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: missense variant
orthologous variants: 165482931-A-G

http://identifiers.org/hco/1/GRCh38#167697789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165482919-C-A

167697810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: missense variant
orthologous variants: 165482898-G-A

167697810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: missense variant
orthologous variants: 165482898-G-T

http://identifiers.org/hco/1/GRCh38#167697813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165482895-C-A

167697813-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: missense variant
orthologous variants: 165482895-C-G

167697813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: stop gained
orthologous variants: 165482895-C-T

167697874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165482849-G-A

167697874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165482849-G-T

167697980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165482762-G-A

167697980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165482762-G-T

167697984-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165482758-A-T

167698609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165482375-C-T

http://identifiers.org/hco/1/GRCh38#167698660-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165482312-A-C

167698796-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165482188-T-G

167698855-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165482132-A-T

167698863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165482119-G-A

167698863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165482119-G-T

167699375-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165481610-T-A

167699899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165481107-T-C

167699899-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165481107-T-G

167700775-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165480267-A-T

http://identifiers.org/hco/1/GRCh38#167701861-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165479560-A-C

167701861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165479560-A-G

167701905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165479536-G-A

167703168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165478876-T-C

167703197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165478844-G-T

167703639-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165478605-C-G

167703660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165478585-A-G

http://identifiers.org/hco/1/GRCh38#167703960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165478441-C-A

167704107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165478334-A-G

167704203-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165478168-T-A

167704293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165478099-G-A

167704293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165478099-G-T

167704318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165478076-A-G

167704435-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165477957-C-G

167704514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165477883-G-T

167704591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165477823-C-T

http://identifiers.org/hco/1/GRCh38#167704652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165477788-C-A

167704652-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: intron variant
orthologous variants: 165477788-C-G

167704685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: missense variant
orthologous variants: 165477756-A-G

http://identifiers.org/hco/1/GRCh38#167704805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165477635-C-A

167704805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: 3 prime UTR variant
orthologous variants: 165477635-C-T

167704814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: 3 prime UTR variant
orthologous variants: 165477626-T-C

167704841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: 3 prime UTR variant
orthologous variants: 165477600-A-G

http://identifiers.org/hco/1/GRCh38#167704848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165477593-C-A

167704848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: 3 prime UTR variant
orthologous variants: 165477593-C-T

167704852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: 3 prime UTR variant
orthologous variants: 165477589-G-A

167704852-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: 3 prime UTR variant
orthologous variants: 165477589-G-C

167704852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: 3 prime UTR variant
orthologous variants: 165477589-G-T

167704897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: 3 prime UTR variant
orthologous variants: 165477547-G-T

167705110-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: 3 prime UTR variant
orthologous variants: 165477390-T-G

http://identifiers.org/hco/1/GRCh38#167705291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165477195-C-A

167705291-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: 3 prime UTR variant
orthologous variants: 165477195-C-G

167705291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: 3 prime UTR variant
orthologous variants: 165477195-C-T

http://identifiers.org/hco/1/GRCh38#167705459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#165476976-C-A

167705482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 165476929-G-A

167705482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 165476929-G-T

167705515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 165476894-A-G

167705599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 165476792-G-T

http://identifiers.org/hco/1/GRCh38#167705715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165476699-C-A

167705715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: 3 prime UTR variant
orthologous variants: 165476699-C-T

167706078-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: 3 prime UTR variant
orthologous variants: 165476344-A-T

167706086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: 3 prime UTR variant
orthologous variants: 165476336-T-C

167706284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: 3 prime UTR variant
orthologous variants: 165476149-T-C

167706358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: 3 prime UTR variant
orthologous variants: 165476103-C-T

167706369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: 3 prime UTR variant
orthologous variants: 165476092-T-C

167706413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: 3 prime UTR variant
orthologous variants: 165476048-G-A

167706519-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: 3 prime UTR variant
orthologous variants: 165475954-A-T

167706553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: 3 prime UTR variant
orthologous variants: 165475928-G-A

167706553-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: 3 prime UTR variant
orthologous variants: 165475928-G-C

167706672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: 3 prime UTR variant
orthologous variants: 165475796-A-G

167706848-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: 3 prime UTR variant
orthologous variants: 165475633-G-C

167706931-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: 3 prime UTR variant
orthologous variants: 165475289-G-C

http://identifiers.org/hco/1/GRCh38#167706993-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28310
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165475230-A-C