16443576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62496529-T-C

16443576-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62496529-T-G

16443601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62496554-G-A

16443601-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62496554-G-C

16443601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62496554-G-T

16443679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62496620-G-A

16443679-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62496620-G-C

16443679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62496620-G-T

http://identifiers.org/hco/17/GRCh38#16443702-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#62496643-A-C

16443702-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62496643-A-T

16443984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 62496925-G-A

16443984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 62496925-G-T

16444053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 62496994-C-T

16444661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62497523-A-G

16447782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62499972-G-A

16447782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62499972-G-T

16448015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62500203-A-G

http://identifiers.org/hco/17/GRCh38#16448018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#62500206-C-A

16448018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62500206-C-T

16448081-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62500253-G-C

16448081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62500253-G-T

16448101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62500273-G-A

16448101-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62500273-G-C

16448177-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62500430-T-A

16448177-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62500430-T-G

16448230-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62500494-T-G

16448395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62500622-G-A

16448395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62500622-G-T

http://identifiers.org/hco/17/GRCh38#16448459-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#62500676-A-C

16448502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62500721-G-A

16448502-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62500721-G-C

16450390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62502996-G-A

16450420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62503023-C-T

16450880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62503344-G-A

16451067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62503688-T-C

16451130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62503749-G-A

16451223-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62503822-G-C

16452968-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62504590-C-G

16452968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62504590-C-T

16455986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62505209-G-A

16456562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62505592-T-C

16456950-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62505925-G-C

16457035-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62506011-A-T

16457056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62506023-T-C

16457171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62506121-C-T

16457193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62506132-C-T

16457263-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62506198-C-G

16459974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 62510213-G-A

16460810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62510824-A-G

16460810-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62510824-A-T

16460837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 62510851-G-A

16460849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62510862-G-T

http://identifiers.org/hco/17/GRCh38#16460857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#62510871-C-A

16460857-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62510871-C-G

http://identifiers.org/hco/17/GRCh38#16460864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#62510878-C-A

16461054-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62511028-G-C

http://identifiers.org/hco/17/GRCh38#16461062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#62511036-C-A

16461067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62511041-T-C

16461162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62511126-T-C

http://identifiers.org/hco/17/GRCh38#16461166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#62511128-C-A

16461166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62511128-C-T

16461216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62511184-A-G

16461216-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62511184-A-T

16461217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62511185-G-T

16462191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62511194-G-A

16462191-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62511194-G-C

16462191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62511194-G-T

16462248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62511251-G-A

16462276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 62511278-G-A

16462312-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 62511314-G-C

http://identifiers.org/hco/17/GRCh38#16462432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#62511427-C-A

http://identifiers.org/hco/17/GRCh38#16462497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#62511483-C-A

16462497-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62511483-C-G

16462497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62511483-C-T

http://identifiers.org/hco/17/GRCh38#16462500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#62511486-C-A

16462500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62511486-C-T

16462506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62511493-G-A

16462523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62511510-T-C

http://identifiers.org/hco/17/GRCh38#16462754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#62511869-C-A

http://identifiers.org/hco/17/GRCh38#16462803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#62511919-C-A

http://identifiers.org/hco/17/GRCh38#16462834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#62511950-C-A

16462834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 62511950-C-T

16462838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62511954-G-A

16462838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62511954-G-T

16462861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62511977-T-C

16464529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62514064-G-A

16464905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62514316-G-A

16465138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62514498-C-T

16465352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62514629-G-T

16465382-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62514660-G-C

16465581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62514813-G-A

16465790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62515018-G-A

16465965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62515155-G-A

16465965-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62515155-G-C

16466525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62515595-C-T

16466737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62515799-G-A

http://identifiers.org/hco/17/GRCh38#16466907-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#62515967-A-C

http://identifiers.org/hco/17/GRCh38#16467032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#62516093-C-A

16467713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62518806-G-A

16468042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62519072-C-T

16468451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62519622-G-A

16468774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62519847-G-A

16469043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62520013-G-A

16469141-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62520132-T-G

16469143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62520134-T-C

16469204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62520173-A-G

http://identifiers.org/hco/17/GRCh38#16469227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#62520200-C-A

16469469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62520428-T-C

16469603-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62520522-G-C

16469830-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62520753-C-G

16469830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62520753-C-T

http://identifiers.org/hco/17/GRCh38#16470351-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#62521205-A-C

16470351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62521205-A-G

http://identifiers.org/hco/17/GRCh38#16470517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#62521409-C-A

16470517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 62521409-C-T

16470560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62521453-G-A

http://identifiers.org/hco/17/GRCh38#16470595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#62521486-C-A

16470595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62521486-C-T

16470605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62521496-T-C

16470682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62521566-G-A

16470682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62521566-G-T

16471086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62521837-C-T

http://identifiers.org/hco/17/GRCh38#16471263-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#62522023-C-A

16471505-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62522147-T-A

16471696-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62522318-C-G

http://identifiers.org/hco/17/GRCh38#16471705-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#62522327-A-C

16474704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62527579-T-C

16475168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62527720-G-A

16475212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62527738-G-A

http://identifiers.org/hco/17/GRCh38#16475213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#62527739-C-A

16475213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62527739-C-T

16477411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 62528338-G-A

16477590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62528464-T-C

16477591-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62528465-T-G

16477674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62528529-C-T

16477744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62528569-T-C

16478057-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62528849-G-C

16478169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62528931-G-A

16478208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62528957-G-T

http://identifiers.org/hco/17/GRCh38#16478525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#62529232-C-A

16478525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62529232-C-T

http://identifiers.org/hco/17/GRCh38#16478543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#62529251-C-A

16478543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62529251-C-T

http://identifiers.org/hco/17/GRCh38#16478571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#62529271-C-A

16478571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62529271-C-T

16478572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62529272-C-T

http://identifiers.org/hco/17/GRCh38#16478591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#62529291-C-A

16478624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62529327-A-G

16478696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62529430-G-A

16478696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62529430-G-T

16478723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62529455-C-T

16478740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62529472-G-T

16478774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62529501-C-T

16478839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62529562-A-G

16479009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62529736-T-C

16479044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62529772-A-G

16479097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62529809-C-T

16480846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron variant
orthologous variants: 62530195-A-G

http://identifiers.org/hco/17/GRCh38#16480871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#62530220-C-A

16481289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron variant
orthologous variants: 62530537-A-G

16481306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron variant
orthologous variants: 62530554-C-T

16482082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron variant
orthologous variants: 62530717-C-T

16482085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron variant
orthologous variants: 62530720-G-A

16482127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron variant
orthologous variants: 62530762-A-G

16482260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron variant
orthologous variants: 62530935-T-C

16482283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron variant
orthologous variants: 62530968-G-A

http://identifiers.org/hco/17/GRCh38#16482323-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#62531008-A-C

16482654-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron variant
orthologous variants: 62531236-G-C

http://identifiers.org/hco/17/GRCh38#16484034-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#62531662-A-C

16484453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron variant
orthologous variants: 62532125-T-C

16484461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron variant
orthologous variants: 62532133-G-A

http://identifiers.org/hco/17/GRCh38#16484511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#62532183-C-A

16484745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, undefined
orthologous variants: 62532522-A-G

http://identifiers.org/hco/17/GRCh38#16484769-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#62532546-A-C

16484769-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron variant
orthologous variants: 62532546-A-T

16485331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 62533507-G-A

16485580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron variant
orthologous variants: 62533650-G-A

16486509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62534126-C-T

16486868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 62534479-G-A

16487844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62535446-A-G

http://identifiers.org/hco/17/GRCh38#16488147-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#62535734-A-C

16488147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62535734-A-G

http://identifiers.org/hco/17/GRCh38#16488571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#62536082-C-A

16488653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 62536164-A-G

16488836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62536334-A-G

http://identifiers.org/hco/17/GRCh38#16488877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#62536351-C-A

16488985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62536441-G-A

16489105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62536533-G-A

http://identifiers.org/hco/17/GRCh38#16489178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#62536601-C-A

16489178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62536601-C-T

16489596-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62537046-T-G

16489678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62537131-G-A

http://identifiers.org/hco/17/GRCh38#16489733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#62537188-C-A

16489984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62537366-G-A

16490541-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62537867-T-G

http://identifiers.org/hco/17/GRCh38#16490956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#62538284-C-A

16490956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62538284-C-T

16491387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62538650-C-T

http://identifiers.org/hco/17/GRCh38#16491520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#62538764-C-A

16491943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 62539169-G-A

16491943-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 62539169-G-C

16491943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 62539169-G-T

http://identifiers.org/hco/17/GRCh38#16492040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#62539262-C-A

16492040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 62539262-C-T

16492087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 62539285-G-A

16492087-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 62539285-G-C

16492087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 62539285-G-T

http://identifiers.org/hco/17/GRCh38#16492155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#62539361-C-A

16492155-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 62539361-C-G

16492155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32403
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 62539361-C-T