163108000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: non coding transcript exon variant
orthologous variants: 67362267-C-T

163108630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: non coding transcript exon variant
orthologous variants: 67361417-G-A

163108630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: non coding transcript exon variant
orthologous variants: 67361417-G-T

163108693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: non coding transcript exon variant
orthologous variants: 67361332-G-A

163108736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: non coding transcript exon variant
orthologous variants: 67361286-C-T

163108803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: non coding transcript exon variant
orthologous variants: 67361216-G-T

163108922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67361180-A-G

163109071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67361029-T-C

http://identifiers.org/hco/4/GRCh38#163109178-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#67360934-A-C

163109178-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67360934-A-T

163109964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67358332-T-C

163110142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 67358262-G-T

163110637-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67358131-A-T

163110690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67358090-G-A

163110702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67358078-A-G

163110932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67357664-C-T

163111201-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67357416-G-C

163115576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67353371-C-T

163115634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67353319-T-C

http://identifiers.org/hco/4/GRCh38#163115789-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#67353173-A-C

163115853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67353090-C-T

163115972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67353004-T-C

163117294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67352769-G-T

163117353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67352719-G-T

163117415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67352671-T-C

163117510-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67352570-T-G

http://identifiers.org/hco/4/GRCh38#163117646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#67352440-C-A

163119201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67349918-G-A

163119202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67349917-T-C

163119849-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67347075-T-A

163119921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67347004-G-A

163119921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67347004-G-T

163119939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67346986-G-A

163119939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67346986-G-T

163119956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67346969-T-C

163120075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67346869-A-G

http://identifiers.org/hco/4/GRCh38#163120112-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#67346832-A-C

http://identifiers.org/hco/4/GRCh38#163120319-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#67346662-A-C

163120688-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67346324-T-G

163120738-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67346264-T-G

163120985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67346088-G-A

163121915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67345448-T-C

163121967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67345386-A-G

163122003-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67345352-G-C

http://identifiers.org/hco/4/GRCh38#163122170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#67345213-C-A

http://identifiers.org/hco/4/GRCh38#163122204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#67345203-C-A

163122777-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67344814-T-G

163127698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67343610-G-A

163127761-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67343553-G-C

163128020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67343331-A-G

163128023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67343328-A-G

163128136-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67343201-A-T

163128306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67343065-C-T

163128552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67342588-A-G

163128567-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67342512-T-A

163128567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67342512-T-C

163128627-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67342448-T-A

163128627-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67342448-T-G

163128632-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67342443-T-A

163128632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67342443-T-C

163128632-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67342443-T-G

163128646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67342434-A-G

163128646-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67342434-A-T

http://identifiers.org/hco/4/GRCh38#163128657-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#67342423-A-C

163128657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67342423-A-G

163128660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67342420-A-G

163128660-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67342420-A-T

163128669-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67342412-T-G

163128694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67342387-A-G

http://identifiers.org/hco/4/GRCh38#163128781-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#67342287-A-C

163128832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67342213-T-C

http://identifiers.org/hco/4/GRCh38#163128879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#67342187-C-A

163128890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67342173-T-C

163128949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 67342113-G-A

163128949-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 67342113-G-C

163128949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 67342113-G-T

163128970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 67342089-G-A

163128970-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 67342089-G-C

163128970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 67342089-G-T

163129057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 67341999-G-A

163129057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 67341999-G-T

163129063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 67341993-G-A

163129063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 67341993-G-T

http://identifiers.org/hco/4/GRCh38#163129072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#67341984-C-A

163129072-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 67341984-C-G

163129072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 67341984-C-T

163129152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 67341904-A-G

163129277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 67341779-G-A

163129277-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 67341779-G-C

163129324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 67341735-T-C

163129452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67341624-G-A

163129452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67341624-G-T

163132613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67341037-G-A

163133064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67340604-A-G

163133064-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67340604-A-T

163133103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67340576-T-C

163133231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 67340448-T-C

163133280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67340400-G-A

163133582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67339990-T-C

163133589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67339983-T-C

http://identifiers.org/hco/4/GRCh38#163134841-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#67339736-A-C

163135296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67339428-A-G

163136636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67338840-C-T

163136653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67338823-C-T

http://identifiers.org/hco/4/GRCh38#163136660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#67338816-C-A

163136752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67338724-G-A

163136823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67338653-T-C

163137072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67338544-G-A

163137072-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67338544-G-C

163137072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67338544-G-T

163137076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67338540-A-G

163137186-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67338479-G-C

163137403-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67338279-G-C

163137414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67338268-C-T

http://identifiers.org/hco/4/GRCh38#163137485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#67338197-C-A

163137669-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67338042-G-C

163137769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67337970-A-G

163137814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67337932-T-C

163137869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67337887-G-A

163138454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67337393-T-C

163138563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67337312-G-A

163138676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67337223-T-C

163138676-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67337223-T-G

163138771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67337141-T-C

163138771-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67337141-T-G

163138792-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67337120-C-G

163139969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67336518-C-T

163140001-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67336486-A-T

163140091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67336385-T-C

163140123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67336354-G-A

163140123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67336354-G-T

http://identifiers.org/hco/4/GRCh38#163140139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#67336338-C-A

163140158-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67336317-T-G

163140209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67336267-G-A

163140283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 67336193-A-G

163140438-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67336041-T-A

http://identifiers.org/hco/4/GRCh38#163140480-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#67336005-A-C

http://identifiers.org/hco/4/GRCh38#163141975-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#67335214-A-C

163141975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67335214-A-G

163141975-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67335214-A-T

163141977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67335212-G-T

163142146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67335045-T-C

http://identifiers.org/hco/4/GRCh38#163142193-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#67334999-A-C

163142766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67333290-C-T

http://identifiers.org/hco/4/GRCh38#163143037-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#67333031-A-C

http://identifiers.org/hco/4/GRCh38#163145162-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#67332874-A-C

163145189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67332847-G-A

163145475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67332588-G-T

163145506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67332563-T-C

163145702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67332392-T-C

163145773-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67332340-T-A

163145884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67332229-A-G

163145970-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67332171-T-A

163145970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67332171-T-C

163145977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67332164-A-G

163145977-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67332164-A-T

163146611-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67331913-T-A

163146611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67331913-T-C

163147996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67330716-G-A

163148008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67330699-C-T

163148055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67330636-T-C

163148056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67330635-T-C

163148217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67330525-T-C

163148310-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67330442-A-T

http://identifiers.org/hco/4/GRCh38#163148484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#67330264-C-A

163148485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67330263-T-C

163148562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67330181-G-A

163148632-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67330123-T-A

163148987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67329810-G-A

163149617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67329255-T-C

163150418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67328767-C-T

163150541-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67328664-T-A

163150541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67328664-T-C

163150909-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67328468-T-A

163151148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67328275-T-C

163151264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67328229-T-C

163151266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67328227-T-C

163151266-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67328227-T-G

163151346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67328189-T-C

163155219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67327397-A-G

http://identifiers.org/hco/4/GRCh38#163155610-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#67327075-C-A

163155610-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67327075-C-G

163156892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67326237-T-C

163156967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67326160-A-G

163157041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67326115-T-C

http://identifiers.org/hco/4/GRCh38#163157079-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#67326077-A-C

http://identifiers.org/hco/4/GRCh38#163157478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#67325745-C-A

163157605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67325487-T-C

163157670-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67325390-T-G

163158205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67324922-T-C

163158263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67324870-T-C

163158366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67324763-T-C

163158598-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67324532-T-A

163159336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67323320-T-C

163159799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67322850-A-G

163160054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67322635-A-G

http://identifiers.org/hco/4/GRCh38#163161087-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#67321515-A-C

163161087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67321515-A-G

163162226-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67320295-A-T

http://identifiers.org/hco/4/GRCh38#163162293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#67320210-C-A

163162891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67318878-T-C

163163514-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67318349-T-A

163163641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67318262-A-G

163163834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67318062-G-A

163164277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 67317290-T-C

http://identifiers.org/hco/4/GRCh38#163164298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#67317269-C-A

163164298-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 67317269-C-G

163164298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 67317269-C-T

163164301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 67317266-C-T

163164347-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 67317226-G-T

163164419-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67317164-T-A

163164419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67317164-T-C

163164464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67317121-A-G

http://identifiers.org/hco/4/GRCh38#163164486-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#67317080-A-C

http://identifiers.org/hco/4/GRCh38#163164517-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#67317050-A-C

163164535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67316982-A-G

http://identifiers.org/hco/4/GRCh38#163164705-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#67316718-A-C

163165076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67316462-C-T

http://identifiers.org/hco/4/GRCh38#163165077-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#67316461-A-C

http://identifiers.org/hco/4/GRCh38#163165375-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#67314709-A-C

163165729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67314424-G-A

163166253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67313780-G-A

163166253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67313780-G-T

163166267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67313765-G-A

163166267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67313765-G-T

163166344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67313715-G-A

163166344-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67313715-G-C

163166432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 67313633-G-A

163166432-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 67313633-G-C

163166432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 67313633-G-T

163166464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 67313584-T-C

http://identifiers.org/hco/4/GRCh38#163166470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#67313578-C-A

163166470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 67313578-C-T

163166481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 67313272-G-A

163166523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 67313230-G-A

163166523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 67313230-G-T

163166528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 67313225-A-G

163166543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 67313210-G-A

163166543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 67313210-G-T

http://identifiers.org/hco/4/GRCh38#163166545-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#67313208-A-C

163166545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 67313208-A-G

163166545-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 67313208-A-T

http://identifiers.org/hco/4/GRCh38#163166554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#67313183-C-A

163166554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 67313183-C-T

http://identifiers.org/hco/4/GRCh38#163166569-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#67313166-A-C

163166577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 67313158-G-A

163166577-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 67313158-G-C

163166577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 67313158-G-T

163166612-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 67313129-C-G

163166619-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 67313122-C-G

163166619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 67313122-C-T

163166785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 67312986-G-A

163166785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 67312986-G-T

163166788-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 67312983-C-G

163166788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 67312983-C-T

http://identifiers.org/hco/4/GRCh38#163166793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#67312978-C-A

163166793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 67312978-C-T

http://identifiers.org/hco/4/GRCh38#163166806-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#67312972-A-C

163166806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 67312972-A-G

163166806-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 67312972-A-T

http://identifiers.org/hco/4/GRCh38#163166829-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#67312950-A-C

163166829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25126
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 67312950-A-G