http://identifiers.org/hco/3/GRCh38#142307232-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#95938924-A-C

142307260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: 3 prime UTR variant
orthologous variants: 95938892-A-G

142307426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: 3 prime UTR variant
orthologous variants: 95938751-C-T

142307606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: 3 prime UTR variant
orthologous variants: 95938582-C-T

142307626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: 3 prime UTR variant
orthologous variants: 95938560-G-T

http://identifiers.org/hco/3/GRCh38#142307662-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#95938524-A-C

142308163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: 3 prime UTR variant
orthologous variants: 95937917-T-C

142308184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: 3 prime UTR variant
orthologous variants: 95937893-A-G

142308434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: 3 prime UTR variant
orthologous variants: 95937687-A-G

142308539-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: 3 prime UTR variant
orthologous variants: 95937526-C-G

142308539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: 3 prime UTR variant
orthologous variants: 95937526-C-T

142308657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: 3 prime UTR variant
orthologous variants: 95937429-G-T

142308901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: 3 prime UTR variant
orthologous variants: 95937193-G-A

142308901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: 3 prime UTR variant
orthologous variants: 95937193-G-T

142309669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: 3 prime UTR variant
orthologous variants: 95936848-G-T

142310243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: 3 prime UTR variant
orthologous variants: 95936355-T-C

142310251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: 3 prime UTR variant
orthologous variants: 95936347-T-C

http://identifiers.org/hco/3/GRCh38#142310416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#95936187-C-A

http://identifiers.org/hco/3/GRCh38#142310429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#95936174-C-A

142310670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: 3 prime UTR variant
orthologous variants: 95935964-A-G

142310670-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: 3 prime UTR variant
orthologous variants: 95935964-A-T

142310924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: 3 prime UTR variant
orthologous variants: 95935580-C-T

http://identifiers.org/hco/3/GRCh38#142310996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#95935495-C-A

142311140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: 3 prime UTR variant
orthologous variants: 95935350-A-G

http://identifiers.org/hco/3/GRCh38#142311506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#95934865-C-A

142311506-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: 3 prime UTR variant
orthologous variants: 95934865-C-G

142311506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: 3 prime UTR variant
orthologous variants: 95934865-C-T

http://identifiers.org/hco/3/GRCh38#142311622-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#95934752-A-C

http://identifiers.org/hco/3/GRCh38#142312547-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#95933849-A-C

http://identifiers.org/hco/3/GRCh38#142312554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#95933844-C-A

142312554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron variant
orthologous variants: 95933844-C-T

http://identifiers.org/hco/3/GRCh38#142312555-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#95933843-A-C

142312555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron variant
orthologous variants: 95933843-A-G

http://identifiers.org/hco/3/GRCh38#142312575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#95933819-C-A

142312814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron variant
orthologous variants: 95933624-G-A

http://identifiers.org/hco/3/GRCh38#142313210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#95933137-C-A

142313363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron variant
orthologous variants: 95932998-G-A

142318915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95929822-G-T

142318995-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95929740-T-A

142319062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95929702-C-T

142319088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95929678-T-C

142329592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 95927560-T-C

142329592-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 95927560-T-G

http://identifiers.org/hco/3/GRCh38#142329654-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#95927500-A-C

142331189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95924927-T-C

http://identifiers.org/hco/3/GRCh38#142331304-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#95924821-A-C

142331677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95924501-G-A

142332301-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95921982-T-A

142332301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95921982-T-C

142332301-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95921982-T-G

142332314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95921969-A-G

142332354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95921924-A-G

142332354-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95921924-A-T

142332377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 95921905-A-G

142332387-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 95921895-T-G

142332413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 95921869-T-C

142332591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95921700-T-C

142332674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95921388-G-A

142332674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95921388-G-T

142332827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95921156-T-C

http://identifiers.org/hco/3/GRCh38#142332848-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#95921133-A-C

142332906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95921080-T-C

142333125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95920899-G-A

http://identifiers.org/hco/3/GRCh38#142333178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#95920860-C-A

142333178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95920860-C-T

142333180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95920858-A-G

http://identifiers.org/hco/3/GRCh38#142333185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#95920853-C-A

142333217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95920823-G-A

142333217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95920823-G-T

142333238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95920789-G-A

142333238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95920789-G-T

142333260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95920767-T-C

142333646-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95920194-G-C

http://identifiers.org/hco/3/GRCh38#142333715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#95920072-C-A

142333895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95919828-G-A

142335189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95917976-G-A

142335350-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95917841-A-T

142335476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 95917719-C-T

142335513-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 95917682-G-C

142335572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron variant
orthologous variants: 95917622-A-G

142347243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: missense variant
orthologous variants: 95915735-G-T

142348089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron variant
orthologous variants: 95914976-G-A

142348232-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron variant
orthologous variants: 95914863-T-G

142348447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron variant
orthologous variants: 95914699-A-G

142348497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron variant
orthologous variants: 95914396-T-C

142348560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron variant
orthologous variants: 95914337-G-A

142351720-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron variant
orthologous variants: 95911541-C-G

142351815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron variant
orthologous variants: 95911638-C-T

142351947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron variant
orthologous variants: 95911690-T-C

142351963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron variant
orthologous variants: 95911705-A-G

http://identifiers.org/hco/3/GRCh38#142351994-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#95911735-A-C

142353241-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron variant
orthologous variants: 95909156-A-T

http://identifiers.org/hco/3/GRCh38#142355280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#95909074-C-A

142355280-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron variant
orthologous variants: 95909074-C-G

142355280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron variant
orthologous variants: 95909074-C-T

142355353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 95909023-A-G

http://identifiers.org/hco/3/GRCh38#142355368-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#95909008-A-C

142355377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 95909003-T-C

142355384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 95908996-A-G

142355424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 95908961-A-G

142355488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 95908897-A-G

142356741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95907184-A-G

http://identifiers.org/hco/3/GRCh38#142356915-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#95906268-A-C

142356920-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 95906263-G-C

142357150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95906044-G-A

142357150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95906044-G-T

142358975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95904784-T-C

142359089-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95904717-G-T

http://identifiers.org/hco/3/GRCh38#142359814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#95903972-C-A

142359814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95903972-C-T

http://identifiers.org/hco/3/GRCh38#142359927-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#95903861-A-C

142359927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 95903861-A-G

142359974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95903816-T-C

142359991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95903800-A-G

142359991-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95903800-A-T

142360082-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95903712-T-A

http://identifiers.org/hco/3/GRCh38#142360097-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#95903700-A-C

142360335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95903294-G-A

142360397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95903194-T-C

142360917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95902861-G-A

142361208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95902579-T-C

142361363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95902461-C-T

142364593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95900865-C-T

142364736-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95900532-T-A

http://identifiers.org/hco/3/GRCh38#142364842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#95900424-C-A

http://identifiers.org/hco/3/GRCh38#142364915-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#95900357-A-C

142364915-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95900357-A-T

http://identifiers.org/hco/3/GRCh38#142364923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#95900349-C-A

142364923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95900349-C-T

http://identifiers.org/hco/3/GRCh38#142364928-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#95900344-A-C

142364928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95900344-A-G

142364928-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95900344-A-T

142364974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95900301-A-G

142365072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 95900205-T-C

142365222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95900053-T-C

http://identifiers.org/hco/3/GRCh38#142365254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#95899954-C-A

142365254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95899954-C-T

142370463-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95893732-C-G

142370463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95893732-C-T

http://identifiers.org/hco/3/GRCh38#142371184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#95893406-C-A

142371222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95893368-T-C

142371351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95893237-T-C

http://identifiers.org/hco/3/GRCh38#142371416-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#95893173-A-C

142371444-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95893146-T-A

142371444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95893146-T-C

142374818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95889634-G-A

142375656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95888995-T-C

142375656-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95888995-T-G

142375725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95888942-T-C

142376315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 95888324-A-G

http://identifiers.org/hco/3/GRCh38#142376633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#95888009-C-A

142376633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95888009-C-T

142376659-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95887983-T-A

142376659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95887983-T-C

142376659-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95887983-T-G

142376693-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95887951-T-A

142377064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95887750-A-G

142379988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95886076-T-C

142380010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95886055-G-A

142380010-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95886055-G-T

142380251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95885819-T-C

142382451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95884991-A-G

142382926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95884603-C-T

142383201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95884389-C-T

142383344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 95884255-T-C

142383373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 95884226-G-A

142383434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95884158-T-C

142383564-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95884042-T-G

142383612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95883996-T-C

142383714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95883905-T-C

142384779-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95881382-A-T

142384814-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95881349-T-A

142397414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 95880313-T-C

http://identifiers.org/hco/3/GRCh38#142397555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#95880170-C-A

142399799-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95878294-T-A

142399799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95878294-T-C

http://identifiers.org/hco/3/GRCh38#142399958-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#95878174-A-C

142400008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95878129-A-G

142400083-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95877599-G-C

142400252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95877422-T-C

142400262-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95877412-G-C

142400300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95877373-G-A

142400300-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95877373-G-C

142400300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95877373-G-T

142400302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95877371-G-A

142400302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95877371-G-T

http://identifiers.org/hco/3/GRCh38#142400304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#95877369-C-A

142400304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95877369-C-T

142400321-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95877361-T-G

142400326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95877356-G-A

142400326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95877356-G-T

142400331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95877351-G-A

142400331-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95877351-G-C

142400331-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95877351-G-T

http://identifiers.org/hco/3/GRCh38#142400509-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#95877189-A-C

142400533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 95877165-T-C

142400555-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 95877142-T-A

142400555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 95877142-T-C

142400555-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 95877142-T-G

http://identifiers.org/hco/3/GRCh38#142400619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#95877079-C-A

http://identifiers.org/hco/3/GRCh38#142400620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#95877078-C-A

142401200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95876798-C-T

142401480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95876556-C-T

142401984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95874718-C-T

142402110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95874158-T-C

142403335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95873618-T-C

142403400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95873561-G-A

142403400-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95873561-G-C

142403489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95873489-G-A

142403489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95873489-G-T

142403558-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95873459-T-G

142403645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95873368-A-G

http://identifiers.org/hco/3/GRCh38#142403653-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#95873360-A-C

142403653-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95873360-A-T

142403659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95873353-A-G

142404123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95872319-A-G

142404268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95871872-C-T

http://identifiers.org/hco/3/GRCh38#142404450-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#95871736-A-C

142404490-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95871672-T-A

142404542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95871630-A-G

142404976-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 95870988-C-G

142404976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 95870988-C-T

142404991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 95870973-A-G

142405112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95870860-T-C

142405113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95870859-A-G

142412495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95867404-T-C

http://identifiers.org/hco/3/GRCh38#142412726-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#95867179-A-C

142412726-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95867179-A-T

142412801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95867145-T-C

142412801-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95867145-T-G

142413597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95865443-G-A

142414127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 95863990-A-G

142414370-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95863753-T-G

142414387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95863736-A-G

http://identifiers.org/hco/3/GRCh38#142414890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#95863452-C-A

142415169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95863171-T-C

142415347-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95862810-G-T

142415367-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95862790-T-A

142415387-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95862771-G-C

142415457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95862704-C-T

142415642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95862545-T-C

142415676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95862506-T-C

http://identifiers.org/hco/3/GRCh38#142417061-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#95861334-A-C

142417061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95861334-A-G

142417061-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95861334-A-T

142417269-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95861141-G-C

http://identifiers.org/hco/3/GRCh38#142417709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#95860803-C-A

142417709-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95860803-C-G

142418092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95860334-T-C

http://identifiers.org/hco/3/GRCh38#142418580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#95859877-C-A

http://identifiers.org/hco/3/GRCh38#142418668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#95859794-C-A

142418668-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95859794-C-G

142418668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95859794-C-T

http://identifiers.org/hco/3/GRCh38#142418686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#95859776-C-A

142418686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95859776-C-T

http://identifiers.org/hco/3/GRCh38#142418729-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#95859738-C-A

142418729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95859738-C-T

142418757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95859702-G-A

142418985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95859369-T-C

http://identifiers.org/hco/3/GRCh38#142419010-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#95859191-A-C

142419010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95859191-A-G

http://identifiers.org/hco/3/GRCh38#142419020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#95859181-C-A

142419926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95858177-G-A

142419937-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95858166-T-A

142419945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95858158-T-C

142421041-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 95856925-T-A

142421041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 95856925-T-C

142421059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 95856907-G-T

142421143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 95856823-T-C

142421202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95856772-G-A

142421202-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95856772-G-C

142421258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95856716-G-A

142421258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95856716-G-T

142421274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95856703-T-C

142421325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95856657-T-C

http://identifiers.org/hco/3/GRCh38#142421330-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#95856652-A-C

http://identifiers.org/hco/3/GRCh38#142421369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#95856618-C-A

142421369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95856618-C-T

http://identifiers.org/hco/3/GRCh38#142421391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#95856596-C-A

142421435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95856553-G-A

http://identifiers.org/hco/3/GRCh38#142421444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#95856545-C-A

142421444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95856545-C-T

142421577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95856414-A-G

142421611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95856379-C-T

142421674-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95856325-T-A

142421674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95856325-T-C

142421674-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95856325-T-G

http://identifiers.org/hco/3/GRCh38#142421682-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#95856317-A-C

142421805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95856201-T-C

142421829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95856184-G-A

142421842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95856171-G-A

142422384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95855827-T-C

142422629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 95855622-A-G

142422771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95855480-A-G

142423028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95855243-T-C

142423109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95855179-T-C

142423457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95852960-G-A

142423457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95852960-G-T

142423507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95852911-A-G

142423553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 95852869-A-G

142423646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 95852776-T-C

142423670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95852752-T-C

142423805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95852621-G-A

http://identifiers.org/hco/3/GRCh38#142424023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#95852457-C-A

142424997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95851831-T-C

142424997-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95851831-T-G

142425081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95851732-A-G

142425083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95851730-T-C

142425123-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95851696-T-G

142425196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95851637-T-C

http://identifiers.org/hco/3/GRCh38#142425418-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#95851404-A-C

142425420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95851402-G-A

142425420-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95851402-G-C

http://identifiers.org/hco/3/GRCh38#142426794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#95849810-C-A

142426794-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 95849810-C-G

142426794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 95849810-C-T

142426864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95849740-T-C

142427434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95849338-T-C

142428602-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95849041-T-G

142428759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95848922-A-G

142428831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95848851-T-C

142429130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95848699-G-A

142429133-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95848696-T-A

142430579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95847342-A-G

142430742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95847179-A-G

142432499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95846374-A-G

142432594-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95846271-T-G

142432778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 95846137-A-G

142433058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95845627-G-A

142446171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95838709-G-A

142446464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95838333-G-A

142446721-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95838156-T-G

142447145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95837659-C-T

142447469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95837353-G-A

142447620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95837208-G-A

http://identifiers.org/hco/3/GRCh38#142447698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#95837151-C-A

142447699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95837150-C-T

http://identifiers.org/hco/3/GRCh38#142447750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#95837100-C-A

142447750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95837100-C-T

http://identifiers.org/hco/3/GRCh38#142447990-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30654
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#95836874-A-C