172420721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 161807217-G-T

172420821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 161807130-G-A

172420876-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 161807083-G-C

172424014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161805737-T-C

172424015-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161805736-G-C

172424029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161805722-T-C

172424310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161805452-A-G

172424871-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161805197-G-C

172424954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161805117-A-G

172425312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161804819-T-C

172425476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161804658-G-A

172429087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161804519-T-C

172429119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161804487-T-C

172429462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161804207-T-C

172429567-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161804113-C-G

172429627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 161804050-T-C

172429775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161803895-G-A

http://identifiers.org/hco/1/GRCh38#172429981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161803095-C-A

172430037-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161803038-G-C

http://identifiers.org/hco/1/GRCh38#172430277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161802810-C-A

172430334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 161802759-A-G

172430334-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 161802759-A-T

172430356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161802740-G-T

172439282-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161801504-C-G

172439290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161801496-A-G

172439401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161801399-G-A

172439514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161801282-C-T

172439561-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161801241-T-A

172439940-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161800871-T-G

172439950-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161800864-T-G

172439970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161800844-C-T

172440765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161799875-C-T

172440786-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161799843-T-A

172441132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161799574-C-T

172441148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161799558-T-C

http://identifiers.org/hco/1/GRCh38#172441166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161799541-C-A

172441350-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161799408-T-A

172441350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161799408-T-C

http://identifiers.org/hco/1/GRCh38#172441354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161799404-C-A

172441354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161799404-C-T

172441404-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161799253-T-A

172441435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161799212-G-T

172441468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 161799182-T-C

172441614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 161799028-T-C

http://identifiers.org/hco/1/GRCh38#172441620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161799022-C-A

172441620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 161799022-C-T

172441674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 161798967-C-T

172441684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 161798957-G-A

172441684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 161798957-G-T

http://identifiers.org/hco/1/GRCh38#172441709-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161798932-A-C

172441720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 161798921-T-C

172441720-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 161798921-T-G

172441808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 161798832-A-G

172441946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 161798694-C-T

172441964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 161798676-A-G

172442093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 161798547-A-G

172442243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 161798397-A-G

172442296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 161798344-C-T

172442468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 161798172-A-G

http://identifiers.org/hco/1/GRCh38#172442669-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161797970-A-C

172442753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 161797891-T-C

http://identifiers.org/hco/1/GRCh38#172442951-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161797707-A-C

172442951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 161797707-A-G

172442961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 161797697-A-G

172443095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 161797596-A-G

172443128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 161797558-G-A

http://identifiers.org/hco/1/GRCh38#172443191-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161797495-A-C

172443272-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 161797418-G-C

172443287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 161797400-T-C

172443324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 161797358-T-C

172443342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 161797339-G-T

172443351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 161797330-G-T

172443363-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 161797323-G-C

http://identifiers.org/hco/1/GRCh38#172443405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161797289-C-A

172443540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 161797151-G-A

http://identifiers.org/hco/1/GRCh38#172443633-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161797088-A-C

http://identifiers.org/hco/1/GRCh38#172443714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161797015-C-A

172443714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 161797015-C-T

http://identifiers.org/hco/1/GRCh38#172443749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161796991-C-A

172443749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 161796991-C-T

172443758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 161796982-A-G

172443758-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 161796982-A-T

http://identifiers.org/hco/1/GRCh38#172443865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161796934-C-A

172443865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 161796934-C-T

http://identifiers.org/hco/1/GRCh38#172443906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161796903-C-A

172443936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 161796872-G-A

172443936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 161796872-G-T

172444013-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 161796816-T-G

172444018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 161796811-G-A

172444018-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 161796811-G-C

172444018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 161796811-G-T

172444029-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 161796800-C-G

172444029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 161796800-C-T

http://identifiers.org/hco/1/GRCh38#172444094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161796728-C-A

172444094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 161796728-C-T

172444138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 161796686-G-A

172444138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 161796686-G-T

172444264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 161796597-G-A

172444264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 161796597-G-T

http://identifiers.org/hco/1/GRCh38#172444406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161796460-C-A

172444931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron variant
orthologous variants: 161795960-T-C

http://identifiers.org/hco/1/GRCh38#172445023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161795864-C-A

http://identifiers.org/hco/1/GRCh38#172445025-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161795818-A-C

172445025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron variant
orthologous variants: 161795818-A-G

http://identifiers.org/hco/1/GRCh38#172445045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161795599-C-A

172445054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron variant
orthologous variants: 161795590-G-A

172445194-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron variant
orthologous variants: 161795444-A-T

172445858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron variant
orthologous variants: 161794848-A-G

172446302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron variant
orthologous variants: 161794486-G-A

172446466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron variant
orthologous variants: 161794326-A-G

172446524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron variant
orthologous variants: 161794275-C-T

http://identifiers.org/hco/1/GRCh38#172446571-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161794232-A-C

http://identifiers.org/hco/1/GRCh38#172446577-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161794226-A-C

172446704-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron variant
orthologous variants: 161794105-G-C

http://identifiers.org/hco/1/GRCh38#172446716-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161794093-C-A

172446993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron variant
orthologous variants: 161793808-G-T

172447040-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron variant
orthologous variants: 161793762-C-G

172447040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron variant
orthologous variants: 161793762-C-T

172447138-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron variant
orthologous variants: 161793662-T-A

172447203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron variant
orthologous variants: 161793588-A-G

http://identifiers.org/hco/1/GRCh38#172447268-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161793521-A-C

172447277-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron variant
orthologous variants: 161793511-G-C

172447618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron variant
orthologous variants: 161793198-G-A

172447618-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron variant
orthologous variants: 161793198-G-C

172447701-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron variant
orthologous variants: 161793133-C-G

172447878-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron variant
orthologous variants: 161792993-T-G

172447937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron variant
orthologous variants: 161792952-C-T

172447938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron variant
orthologous variants: 161792951-A-G

172447938-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron variant
orthologous variants: 161792951-A-T

172448211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron variant
orthologous variants: 161792696-T-C

172448401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron variant
orthologous variants: 161792513-G-A

172448406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron variant
orthologous variants: 161792508-T-C

http://identifiers.org/hco/1/GRCh38#172448452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161792462-C-A

172448452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 161792462-C-T

172448585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron variant
orthologous variants: 161792289-G-A

172448585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron variant
orthologous variants: 161792289-G-T

http://identifiers.org/hco/1/GRCh38#172448666-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161792201-A-C

172448666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron variant
orthologous variants: 161792201-A-G

172448666-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron variant
orthologous variants: 161792201-A-T

172448868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron variant
orthologous variants: 161791959-G-A

172448967-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron variant
orthologous variants: 161791867-C-G

172449111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron variant
orthologous variants: 161791732-G-A

172449304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron variant
orthologous variants: 161791557-G-A

172449350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron variant
orthologous variants: 161791505-T-C

172449882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron variant
orthologous variants: 161791081-T-C

172449943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron variant
orthologous variants: 161791021-C-T

172450234-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, undefined
orthologous variants: 161790637-T-G

172450440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron variant
orthologous variants: 161790443-G-A

172450476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, undefined
orthologous variants: 161790413-G-A

172450899-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, undefined
orthologous variants: 161789994-T-G

172451576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161789421-A-G

172451717-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161789309-T-A

172451817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161789253-C-T

172452315-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161788927-A-T

http://identifiers.org/hco/1/GRCh38#172452727-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161788522-A-C

http://identifiers.org/hco/1/GRCh38#172452840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161788421-C-A

http://identifiers.org/hco/1/GRCh38#172452883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#161788379-C-A

172452883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 161788379-C-T

http://identifiers.org/hco/1/GRCh38#172452896-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161788366-C-A

172452896-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 161788366-C-G

172452933-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 161788332-G-C

172453003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 161788269-G-A

172453039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 161788221-T-C

172453063-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 161788196-T-G

172453098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 161788161-T-C

172453118-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 161788144-C-G

172453139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 161788125-A-G

172454630-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161787249-T-G

172454674-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161787204-C-G

172454743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161787110-C-T

http://identifiers.org/hco/1/GRCh38#172454766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161787090-C-A

172454805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161787060-G-A

172454848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161786662-T-C

172454954-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161786578-C-G

172455004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161786548-G-A

172455004-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161786548-G-C

172455136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161786420-C-T

172455293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161785768-G-A

172455435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161785649-T-C

172455629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161785448-T-C

http://identifiers.org/hco/1/GRCh38#172456069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161785075-C-A

172456220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161784930-C-T

172456286-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161784863-G-C

172456286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161784863-G-T

172456293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161784856-C-T

172456315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161784834-A-G

172456350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161784807-T-C

http://identifiers.org/hco/1/GRCh38#172456365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161784792-C-A

172456366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161784791-T-C

172456398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161784759-T-C

172456404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161784754-T-C

172456443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 161784715-T-C

http://identifiers.org/hco/1/GRCh38#172456469-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161784689-A-C

http://identifiers.org/hco/1/GRCh38#172456486-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161784663-A-C

172456486-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 161784663-A-T

172456578-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161784572-A-T

http://identifiers.org/hco/1/GRCh38#172457647-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161783651-A-C

172457647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161783651-A-G

172457887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161783425-T-C

172461165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161781016-C-T

172461197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161780977-C-T

172461472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161780777-A-G

172461487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161780763-A-G

172461584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161780669-C-T

172461712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161780549-A-G

172461787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161780459-A-G

172461898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161780364-C-T

172462257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161780155-A-G

172462272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161780140-T-C

172462339-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161780082-T-A

172462339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161780082-T-C

172462558-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161779873-G-C

172463191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161779389-A-G

172463309-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161779285-C-G

172463715-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161778914-T-A

172464047-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161778500-T-G

172464077-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161778373-A-T

172464134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161778323-G-A

172464201-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161778260-A-T

http://identifiers.org/hco/1/GRCh38#172464223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161778238-C-A

172464463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161777808-T-C

http://identifiers.org/hco/1/GRCh38#172464957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161777565-C-A

http://identifiers.org/hco/1/GRCh38#172465243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161777265-C-A

172465243-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161777265-C-G

http://identifiers.org/hco/1/GRCh38#172465261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161777246-C-A

172465261-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161777246-C-G

172465261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161777246-C-T

172465273-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161777234-T-A

172465390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161777120-G-A

172465423-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161777088-T-A

172465445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161777065-A-G

172465452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161777058-A-G

http://identifiers.org/hco/1/GRCh38#172465482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161777028-C-A

172465482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161777028-C-T

172465491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161777018-T-C

172465543-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161776910-T-A

http://identifiers.org/hco/1/GRCh38#172465588-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161776869-A-C

172465588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161776869-A-G

http://identifiers.org/hco/1/GRCh38#172465599-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161776858-C-A

172465599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 161776858-C-T

172468386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161770163-G-A

172468386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 161770163-G-T

http://identifiers.org/hco/1/GRCh38#172468420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161770132-C-A

172468464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 161770087-G-A

172468464-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 161770087-G-C

172468464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 161770087-G-T

172468490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 161770061-G-A

172468490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 161770061-G-T

172468525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 161770026-A-G

172468535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 161770016-G-A

172468545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 161770006-G-A

http://identifiers.org/hco/1/GRCh38#172468589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161769958-C-A

172468589-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 161769958-C-G

http://identifiers.org/hco/1/GRCh38#172468603-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161769944-A-C

172468647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 161769896-A-G

http://identifiers.org/hco/1/GRCh38#172468679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161769864-C-A

172468679-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 161769864-C-G

http://identifiers.org/hco/1/GRCh38#172468690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161769859-C-A

172468690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 161769859-C-T

172468707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 161769842-T-C

172468709-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 161769840-T-A

172468709-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 161769840-T-G

http://identifiers.org/hco/1/GRCh38#172468731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#161769820-C-A

172468731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 161769820-C-T

172468785-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29591
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 161769780-T-G