http://identifiers.org/hco/9/GRCh38#132944004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#28531828-C-A

http://identifiers.org/hco/9/GRCh38#132944029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#28531795-C-A

132944029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 28531795-C-T

http://identifiers.org/hco/9/GRCh38#132944034-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#28531790-A-C

132944034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 28531790-A-G

http://identifiers.org/hco/9/GRCh38#132944086-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#28531738-C-A

http://identifiers.org/hco/9/GRCh38#132944104-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#28531723-A-C

132944113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28531714-T-C

132944122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28531705-T-C

132944391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28531468-G-A

http://identifiers.org/hco/9/GRCh38#132944413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#28531447-C-A

132944655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 28531217-G-A

132944671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 28531201-A-G

132944686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 28531186-G-A

132944686-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 28531186-G-C

132944686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 28531186-G-T

132944761-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 28531112-C-G

132944761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 28531112-C-T

132945112-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28530769-C-G

132945112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28530769-C-T

132946139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28528190-C-T

132946140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28528189-G-A

132946178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28528151-G-A

132946506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28527873-G-T

http://identifiers.org/hco/9/GRCh38#132946604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28527795-C-A

132946604-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28527795-C-G

http://identifiers.org/hco/9/GRCh38#132946620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28527779-C-A

132946620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28527779-C-T

132946621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28527778-A-G

132946637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28527762-T-C

132946641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28527758-G-T

132946691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28527715-A-G

132946700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28527711-G-A

132946700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28527711-G-T

132946740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28527694-A-G

132946749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28527685-A-G

132946749-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28527685-A-T

132946851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28527590-G-A

132946899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28527542-A-G

132946943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28527500-A-G

132947004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28527444-G-A

132947004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28527444-G-T

132947033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28527434-G-A

132947107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 28527401-T-C

http://identifiers.org/hco/9/GRCh38#132947173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28527357-C-A

132947173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 28527357-C-T

132947305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28527240-C-T

132970458-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron variant
orthologous variants: 28520848-C-G

132970616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron variant
orthologous variants: 28520636-G-A

132970962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron variant
orthologous variants: 28520258-C-T

132971571-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron variant
orthologous variants: 28518525-A-T

http://identifiers.org/hco/9/GRCh38#132971660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28518424-C-A

http://identifiers.org/hco/9/GRCh38#132972692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#28518312-C-A

132972692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, undefined
orthologous variants: 28518312-C-T

132972801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, undefined
orthologous variants: 28518221-G-A

132972801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, undefined
orthologous variants: 28518221-G-T

132972895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron variant
orthologous variants: 28518189-T-C

http://identifiers.org/hco/9/GRCh38#132973001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28518062-C-A

132973001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron variant
orthologous variants: 28518062-C-T

132973112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron variant
orthologous variants: 28517960-A-G

http://identifiers.org/hco/9/GRCh38#132973124-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28517948-A-C

132973124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron variant
orthologous variants: 28517948-A-G

132975890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron variant
orthologous variants: 28513864-G-A

132976019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron variant
orthologous variants: 28513762-G-T

132976036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron variant
orthologous variants: 28513754-G-A

132976335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron variant
orthologous variants: 28513515-A-G

132976350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron variant
orthologous variants: 28513500-A-G

http://identifiers.org/hco/9/GRCh38#132976422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28513423-C-A

132976430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron variant
orthologous variants: 28513415-G-A

132976499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: 5 prime UTR variant
orthologous variants: 28513330-G-A

132976525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: 5 prime UTR variant
orthologous variants: 28513305-G-A

132976525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: 5 prime UTR variant
orthologous variants: 28513305-G-T

132976535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: 5 prime UTR variant
orthologous variants: 28513295-G-A

132976535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: 5 prime UTR variant
orthologous variants: 28513295-G-T

132976571-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: 5 prime UTR variant
orthologous variants: 28513268-T-A

132976571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: 5 prime UTR variant
orthologous variants: 28513268-T-C

132977715-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron variant
orthologous variants: 28512784-T-A

132977715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron variant
orthologous variants: 28512784-T-C

132977935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron variant
orthologous variants: 28512598-C-T

132977961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, undefined
orthologous variants: 28512554-G-A

132978124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron variant
orthologous variants: 28512400-C-T

132978186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron variant
orthologous variants: 28512344-G-A

132978622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 28512068-G-A

132978756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 28511938-G-A

132978756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 28511938-G-T

http://identifiers.org/hco/9/GRCh38#132978798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#28511902-C-A

132978798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 28511902-C-T

132978809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 28511891-G-A

132978809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 28511891-G-T

132978848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 28511852-G-T

132978878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28511822-T-C

132978899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28511798-A-G

http://identifiers.org/hco/9/GRCh38#132979033-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28511666-A-C

132979039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28511657-T-C

132979556-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28511391-T-G

132979587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28511360-A-G

132979589-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28511358-T-G

132979639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28511334-G-A

132979736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28511247-A-G

132979881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28511129-A-G

http://identifiers.org/hco/9/GRCh38#132979892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28511115-C-A

http://identifiers.org/hco/9/GRCh38#132982355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28508928-C-A

132982669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28508628-T-C

132982784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28508519-G-A

132983024-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28508323-C-G

132983024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28508323-C-T

132983086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28508269-A-G

132984580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28507463-C-T

132984634-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28507417-C-G

132984634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28507417-C-T

132984651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28507399-G-T

132984818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28507264-G-A

132985022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28507078-T-C

132985130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28506984-C-T

132985184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28506933-G-A

132985410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28506735-C-T

132985567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28506588-G-A

132985567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28506588-G-T

132985682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28506468-T-C

132985725-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28506424-T-A

132986088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28505850-A-G

132986377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28505634-C-T

132986518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28505532-C-T

http://identifiers.org/hco/9/GRCh38#132986669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28505397-C-A

132986669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 28505397-C-T

http://identifiers.org/hco/9/GRCh38#132986730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28505335-C-A

132986730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 28505335-C-T

http://identifiers.org/hco/9/GRCh38#132986800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28505261-C-A

132986800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28505261-C-T

132986890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28505182-A-G

132987374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 28504810-G-A

132987471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28504716-G-A

132987479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28504701-G-A

132987523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28504658-A-G

132987540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28504646-A-G

132987596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28504593-C-T

132987691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28504498-T-C

132988167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28503983-G-A

132988287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 28503868-C-T

132988481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28503663-G-A

http://identifiers.org/hco/9/GRCh38#132988493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28503651-C-A

132988493-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28503651-C-G

132988493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28503651-C-T

132988509-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28503635-T-A

132988509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28503635-T-C

http://identifiers.org/hco/9/GRCh38#132988510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28503634-C-A

http://identifiers.org/hco/9/GRCh38#132988548-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28503598-C-A

132988548-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28503598-C-G

132988548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28503598-C-T

132988551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28503595-T-C

132988551-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28503595-T-G

132988573-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28503573-T-A

132988573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28503573-T-C

132988573-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28503573-T-G

132988587-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28503567-A-T

http://identifiers.org/hco/9/GRCh38#132988603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28503553-C-A

132988603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28503553-C-T

http://identifiers.org/hco/9/GRCh38#132988631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28503537-C-A

132988631-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28503537-C-G

132988631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28503537-C-T

132988632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28503536-G-A

132988660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28503516-A-G

132988862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28503098-G-A

132989067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 28502922-T-C

http://identifiers.org/hco/9/GRCh38#132989206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28502783-C-A

132989206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 28502783-C-T

132989535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28501850-G-A

132989535-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28501850-G-C

132989535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28501850-G-T

132989594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28501791-C-T

http://identifiers.org/hco/9/GRCh38#132989602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28501787-C-A

132989602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28501787-C-T

http://identifiers.org/hco/9/GRCh38#132989603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28501786-C-A

http://identifiers.org/hco/9/GRCh38#132989640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28501729-C-A

132989640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 28501729-C-T

132989676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 28501693-G-A

132989676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 28501693-G-T

http://identifiers.org/hco/9/GRCh38#132989697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28501672-C-A

http://identifiers.org/hco/9/GRCh38#132989745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28501591-C-A

132989745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 28501591-C-T

132989784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 28501552-C-T

132990778-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28500291-T-A

132990778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28500291-T-C

http://identifiers.org/hco/9/GRCh38#132990818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28500258-C-A

http://identifiers.org/hco/9/GRCh38#132991076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28500025-C-A

132991076-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 28500025-C-G

132991076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 28500025-C-T

http://identifiers.org/hco/9/GRCh38#132991084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28500018-C-A

132991084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 28500018-C-T

132991148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 28499950-G-A

132991148-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 28499950-G-T

http://identifiers.org/hco/9/GRCh38#132991154-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28499944-A-C

http://identifiers.org/hco/9/GRCh38#132991162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28499936-C-A

http://identifiers.org/hco/9/GRCh38#132991314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28499811-C-A

http://identifiers.org/hco/9/GRCh38#132991315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28499810-C-A

132991315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28499810-C-T

http://identifiers.org/hco/9/GRCh38#132991346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28499779-C-A

132991346-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28499779-C-G

132991370-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28499761-T-A

132991514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28499639-G-A

132991515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28499638-G-A

132991515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28499638-G-T

132991536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28499618-G-A

132991573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28499582-G-A

132991573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28499582-G-T

132991596-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28499560-C-G

http://identifiers.org/hco/9/GRCh38#132991608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28499548-C-A

132991608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28499548-C-T

132991624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4238
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28499532-C-T