http://identifiers.org/hco/8/GRCh38#19313715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68729407-C-A

19313715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 68729407-C-T

19313723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 68729422-G-A

19313723-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 68729422-G-C

19313723-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 68729422-G-T

19313777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 68729481-G-T

19313788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 68729492-T-C

19313788-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 68729492-T-G

http://identifiers.org/hco/8/GRCh38#19313792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68729496-C-A

19313792-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 68729496-C-G

19313792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 68729496-C-T

19313832-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68729551-T-A

19313832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68729551-T-C

19313832-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68729551-T-G

19313873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68729589-G-T

19313888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68729620-G-A

19313888-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68729620-G-T

19313918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 68729646-G-A

19313918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 68729646-G-T

19313995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68729721-A-G

http://identifiers.org/hco/8/GRCh38#19314028-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68729752-C-A

http://identifiers.org/hco/8/GRCh38#19314043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68729767-C-A

http://identifiers.org/hco/8/GRCh38#19314176-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68729902-C-A

19314176-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68729902-C-G

http://identifiers.org/hco/8/GRCh38#19314307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68730095-C-A

19314324-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68730109-G-C

19314430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 68730208-G-T

19314441-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 68730219-C-G

19314560-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68730343-T-A

19314560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68730343-T-C

19314640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68730408-A-G

19314672-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68730440-A-T

19314819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68730560-C-T

19315491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68730780-G-A

19315491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68730780-G-T

19315631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68730913-G-A

http://identifiers.org/hco/8/GRCh38#19315875-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68731147-A-C

19315875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68731147-A-G

19315964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68731228-G-A

19316145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68731344-A-G

19316201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68731379-G-A

19316306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68731561-A-G

19316457-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68731777-T-G

http://identifiers.org/hco/8/GRCh38#19316508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68731839-C-A

19316530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68731860-G-A

19317147-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68732416-C-G

19317345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68732666-G-A

http://identifiers.org/hco/8/GRCh38#19317364-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68732685-A-C

19317458-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68732800-G-C

19317657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68732981-C-T

19317759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68733048-A-G

19318503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68733778-T-C

19318760-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68734028-C-G

19318766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68734034-T-C

19318878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68734207-C-T

19318899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68734255-T-C

19318902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68734258-G-A

19318904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68734260-T-C

19318952-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68734317-T-G

19318961-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68734326-C-G

19319107-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68734484-A-T

19319286-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 68734637-T-A

19319287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68734638-A-G

19319313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68734655-C-T

http://identifiers.org/hco/8/GRCh38#19319347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68734698-C-A

http://identifiers.org/hco/8/GRCh38#19319423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68734760-C-A

19319423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 68734760-C-T

http://identifiers.org/hco/8/GRCh38#19319436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68734773-C-A

19319436-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 68734773-C-G

19319436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 68734773-C-T

19319443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 68734780-G-T

19319444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 68734781-G-A

19319444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 68734781-G-T

http://identifiers.org/hco/8/GRCh38#19319607-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68734942-C-A

19319607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 68734942-C-T

19319752-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68735084-G-C

http://identifiers.org/hco/8/GRCh38#19319811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68735132-C-A

http://identifiers.org/hco/8/GRCh38#19319822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68735143-C-A

19320190-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68735584-C-G

19320191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68735585-T-C

19320191-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68735585-T-G

19320273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68735671-A-G

19320327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68735726-A-G

19320870-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68735912-G-C

19320924-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68735965-G-T

19321877-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68737013-C-G

19321893-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68737045-A-T

19323925-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68739643-G-C

http://identifiers.org/hco/8/GRCh38#19324115-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68739766-A-C

19324115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68739766-A-G

19324166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68739809-T-C

19324188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68739831-G-A

http://identifiers.org/hco/8/GRCh38#19324319-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68739950-A-C

19325041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68740681-G-A

19325121-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68740759-G-C

19325121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68740759-G-T

19325354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68741003-A-G

19325392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68741040-T-C

19325431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68741079-A-G

19325484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68741138-A-G

19325669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68741285-T-C

19325708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68741323-G-A

19325727-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68741341-T-G

19325744-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68741361-A-T

19325887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68741494-T-C

http://identifiers.org/hco/8/GRCh38#19326260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68741837-C-A

19327047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68742394-C-T

19327141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68742513-G-T

19327152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68742525-G-A

19327152-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68742525-G-C

19327163-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68742536-C-G

19327163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68742536-C-T

19327413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68742784-C-T

19327418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68742789-G-A

19327476-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68742838-T-A

19327476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68742838-T-C

19330462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68745259-A-G

19330631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68745420-G-A

19330631-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68745420-G-C

19330732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68745517-A-G

http://identifiers.org/hco/8/GRCh38#19330763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68745545-C-A

19330763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68745545-C-T

19331077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68745870-G-A

19331077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68745870-G-T

http://identifiers.org/hco/8/GRCh38#19331328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68746097-C-A

19331329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68746098-C-T

19331381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68746141-G-A

19331452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68746172-G-A

19331453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68746173-G-A

19331453-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68746173-G-C

19331493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68746213-G-A

http://identifiers.org/hco/8/GRCh38#19331770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68746482-C-A

19332719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68746771-G-A

19332719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68746771-G-T

http://identifiers.org/hco/8/GRCh38#19332724-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68746776-A-C

http://identifiers.org/hco/8/GRCh38#19332829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68746854-C-A

19332829-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68746854-C-G

19332829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68746854-C-T

19333080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 68747080-C-T

19333118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68747115-T-C

19333126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68747123-G-T

19333178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68747415-C-T

http://identifiers.org/hco/8/GRCh38#19333182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68747419-C-A

19333182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68747419-C-T

http://identifiers.org/hco/8/GRCh38#19333189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68747426-C-A

19333200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68747437-A-G

19333208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68747445-G-A

19333208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68747445-G-T

19333590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68748205-G-A

19333659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68748274-G-T

19333745-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68748379-C-G

http://identifiers.org/hco/8/GRCh38#19333874-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68748511-C-A

19334140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68748773-G-A

19334315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68748889-T-C

19334449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68749019-C-T

http://identifiers.org/hco/8/GRCh38#19334556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68749124-C-A

19334556-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68749124-C-G

19334556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68749124-C-T

19334595-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68749179-T-G

19334665-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68749275-T-A

http://identifiers.org/hco/8/GRCh38#19334747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68749367-C-A

19334753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 68749373-C-T

19334760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 68749380-A-G

19334769-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 68749389-C-G

19334769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 68749389-C-T

19335332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68749667-G-A

19335590-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68749910-T-G

19335681-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68749999-T-A

19335681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68749999-T-C

19335705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68750029-C-T

19335780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68750103-G-T

19335783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68750106-T-C

19335939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68750272-A-G

19336030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68750368-C-T

19336096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68750420-G-A

http://identifiers.org/hco/8/GRCh38#19341069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68758900-C-A

19341072-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68758903-T-G

http://identifiers.org/hco/8/GRCh38#19341097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68758927-C-A

http://identifiers.org/hco/8/GRCh38#19343462-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68760037-A-C

19343490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68760065-G-A

19343490-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68760065-G-C

19343520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68760072-A-G

19343671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68760193-G-A

19343671-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68760193-G-C

19343671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68760193-G-T

19343684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68760205-G-T

19343715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68760236-C-T

19343758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68760277-G-A

19343841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68760356-T-C

19343915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68760437-A-G

19345802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68763485-A-G

19345837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68763520-C-T

http://identifiers.org/hco/8/GRCh38#19345863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68763548-C-A

19345871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68763556-A-G

19345880-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68763565-G-C

19345948-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68763636-C-G

19346014-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68763700-A-T

19348829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68764449-G-A

19348904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68764517-C-T

19348952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68764577-G-A

19348980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68764616-A-G

http://identifiers.org/hco/8/GRCh38#19349203-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68764826-A-C

19349235-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68764865-G-C

19349339-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68764942-T-G

19349544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68765148-A-G

19349595-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68765198-T-G

http://identifiers.org/hco/8/GRCh38#19349659-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68765261-A-C

19349691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68765284-A-G

http://identifiers.org/hco/8/GRCh38#19350835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68772451-C-A

19350951-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68772568-G-C

19350960-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68772577-C-G

19351651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68773116-G-T

19352524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68773655-A-G

19352698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68773827-C-T

http://identifiers.org/hco/8/GRCh38#19353086-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68773873-A-C

19353269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68774032-C-T

19353651-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68774097-G-C

19353754-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68774188-G-C

19353778-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68774223-C-G

19353784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68774229-G-A

19353894-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68774336-G-C

19353902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68774344-G-T

19354496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68774553-G-A

19354496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68774553-G-T

http://identifiers.org/hco/8/GRCh38#19354828-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68774866-A-C

19354889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68774923-G-A

19355061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68775039-T-C

19355207-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68775078-T-A

19355222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68775097-G-A

19355261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68775136-T-C

19355332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68775200-T-C

19355403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68775254-C-T

19355438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68775290-C-T

19355456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68775308-A-G

19355456-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68775308-A-T

19355545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68776032-C-T

19355857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68776275-C-T

19355886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68776302-T-C

19355886-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68776302-T-G

19355921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68776337-A-G

19355941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68776349-A-G

19356957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68776506-C-T

19357074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68776629-G-T

http://identifiers.org/hco/8/GRCh38#19357253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68776781-C-A

http://identifiers.org/hco/8/GRCh38#19357314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68776833-C-A

19357314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68776833-C-T

19357516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68777034-A-G

19357535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68777053-C-T

19357536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68777054-G-A

19357547-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68777065-C-G

19357582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68777100-A-G

19357776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68777315-G-A

19358008-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68777553-A-T

19359230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68778875-A-G

19359230-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68778875-A-T

19359525-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68780286-G-C

19359663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68780429-G-A

19360668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68781448-G-A

19360668-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68781448-G-C

19360668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68781448-G-T

19360702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68781479-G-T

19360703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68781480-A-G

19360818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68781566-G-A

19360818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68781566-G-T

19360856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68781602-T-C

19360908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68781652-T-C

19360956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68781696-G-A

19360956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68781696-G-T

19360975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68781715-G-T

http://identifiers.org/hco/8/GRCh38#19361035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68781773-C-A

19361035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68781773-C-T

19361130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68781857-G-A

19361130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68781857-G-T

19361165-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68781881-G-T

19361166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68781882-T-C

http://identifiers.org/hco/8/GRCh38#19361200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68781898-C-A

http://identifiers.org/hco/8/GRCh38#19361213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68781911-C-A

19361213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 68781911-C-T

19361215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 68781913-A-G

19361217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 68781915-G-A

19361217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 68781915-G-T

http://identifiers.org/hco/8/GRCh38#19361327-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68782024-A-C

19361327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 68782024-A-G

http://identifiers.org/hco/8/GRCh38#19361369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68782066-C-A

19361369-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68782066-C-G

19361369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68782066-C-T

19361380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68782075-G-A

19361380-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68782075-G-C

19361380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68782075-G-T

19361381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68782076-A-G

19361413-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68782108-G-C

19361413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68782108-G-T

http://identifiers.org/hco/8/GRCh38#19361454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68782148-C-A

19361579-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68782260-G-C

19361591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68782272-G-A

19361919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68782686-T-C

19362325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68783059-G-A

19362334-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68783081-G-C

http://identifiers.org/hco/8/GRCh38#19363763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68783359-C-A

19363763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68783359-C-T

http://identifiers.org/hco/8/GRCh38#19363907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68783512-C-A

19364036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68783641-T-C

http://identifiers.org/hco/8/GRCh38#19364197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68783803-C-A

19364197-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 68783803-C-G

19364197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 68783803-C-T

19364327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68783933-G-A

19364355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68783946-G-A

19364386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68783974-G-A

19364386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68783974-G-T

19364406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68783992-A-G

http://identifiers.org/hco/8/GRCh38#19364429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68784016-C-A

19364429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68784016-C-T

19364517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68784083-T-C

19364642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68784164-T-C

19364753-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68784247-A-T

19364971-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68784448-C-G

19365059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68784561-G-A

19365277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68784778-G-A

19365277-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68784778-G-C

19365451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68784897-G-A

19365460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68784902-G-T

19365483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68784921-G-T

http://identifiers.org/hco/8/GRCh38#19365486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68784924-C-A

19365486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68784924-C-T

http://identifiers.org/hco/8/GRCh38#19365713-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68785129-A-C

19365796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68785188-G-A

19365855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68785261-C-T

19365973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68785379-G-A

19365980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68785386-A-G

19366024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68785430-A-G

19372653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68785635-A-G

19372738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68785719-G-T

19372777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68785755-C-T

19372888-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68785854-A-T

19372950-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68785918-T-A

19372998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68785965-T-C

19372999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68785966-A-G

19373025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68785992-G-A

19373025-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68785992-G-C

19373062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68786013-C-T

19373149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68786088-A-G

19373216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68786132-G-A

19373235-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68786151-T-A

19373473-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68787660-G-C

19373473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68787660-G-T

19373508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68787694-G-T

19373556-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68787743-C-G

19373559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68787746-G-A

19373742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68787919-G-T

19373751-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68787937-T-G

19373754-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68787940-T-G

19373760-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68787946-T-G

19373761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68787947-G-A

19373761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68787947-G-T

http://identifiers.org/hco/8/GRCh38#19373762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68787948-C-A

19373762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68787948-C-T

19373786-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68787971-T-A

19373885-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68788071-G-C

http://identifiers.org/hco/8/GRCh38#19373997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68788179-C-A

19373998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68788180-A-G

19374086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68788291-G-A

19374130-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68788338-G-C

19374398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68788993-T-C

19374477-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68789046-T-G

http://identifiers.org/hco/8/GRCh38#19374564-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68789132-A-C

19374642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68789207-C-T

19374676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68789240-T-C

19374741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68789292-A-G

19374847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68789367-G-A

19374925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68789448-T-C

19374966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68789493-A-G

http://identifiers.org/hco/8/GRCh38#19375068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68789628-C-A

19375081-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68789644-G-C

http://identifiers.org/hco/8/GRCh38#19375091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68789654-C-A

19375091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68789654-C-T

19375126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68789689-A-G

19375161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68789733-T-C

19375342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68789921-T-C

19383787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68791421-G-A

19383868-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68791509-C-G

19383923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68791558-A-G

19384244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68791902-G-A

19384586-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68792246-C-G

19384957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68792605-T-C

19385062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68792701-T-C

19385062-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68792701-T-G

19385126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68792749-A-G

19385178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68792801-G-A

19385194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68792816-A-G

http://identifiers.org/hco/8/GRCh38#19385200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68792822-C-A

19385320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68792858-C-T

http://identifiers.org/hco/8/GRCh38#19385647-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68792983-A-C

http://identifiers.org/hco/8/GRCh38#19385653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68792989-C-A

19385653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68792989-C-T

19385913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68793175-G-A

19385935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68793200-C-T

19386029-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68793290-C-G

19386197-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68793474-T-G

19386250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68793529-C-T

http://identifiers.org/hco/8/GRCh38#19386378-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68793645-A-C

19386378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68793645-A-G

19386404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68793671-A-G

19386411-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68793678-A-T

19386414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68793681-G-A

19388510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68795480-A-G

http://identifiers.org/hco/8/GRCh38#19388532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68795513-C-A

19388532-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68795513-C-G

19388532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68795513-C-T

19388611-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68795593-A-T

19388671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68795643-G-A

19388702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68795670-T-C

19388745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68795695-C-T

http://identifiers.org/hco/8/GRCh38#19388798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68795725-C-A

19389043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68795892-G-A

19389106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68795944-C-T

19389224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68796057-G-A

19389526-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68796419-C-G

19389564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68796458-G-A

19389564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68796458-G-T

http://identifiers.org/hco/8/GRCh38#19389582-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68796476-A-C

19389598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68796492-C-T

19389624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68796505-G-A

19389662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68796536-A-G

19389703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68796577-T-C

http://identifiers.org/hco/8/GRCh38#19389761-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68796596-C-A

19389767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68796602-A-G

19389859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68796676-G-A

19390554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68797078-A-G

19390568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68797092-A-G

19390886-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68797410-C-G

19390886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68797410-C-T

19391000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68797526-G-T

19392626-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68797911-C-G

19392740-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68798040-T-G

19393209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68798506-G-A

19393209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68798506-G-T

http://identifiers.org/hco/8/GRCh38#19393245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68798536-C-A

19393245-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68798536-C-G

19393291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68798581-T-C

19393331-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 68798618-C-G

19393331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: non_coding_transcript_exon_variant, stop_gained, synonymous_variant
orthologous variants: 68798618-C-T

19393362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 68798646-G-A

19393362-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 68798646-G-C

http://identifiers.org/hco/8/GRCh38#19393370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68798654-C-A

19393370-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 68798654-C-G

19393370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 68798654-C-T

http://identifiers.org/hco/8/GRCh38#19393403-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68798687-C-A

19393403-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 68798687-C-G

19393403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 68798687-C-T

19393454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 68798738-C-T

19393551-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68798835-T-A

19393551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68798835-T-C

http://identifiers.org/hco/8/GRCh38#19393584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68798868-C-A

19393608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68798894-G-A

19393608-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68798894-G-C

19393608-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68798894-G-T

http://identifiers.org/hco/8/GRCh38#19393653-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68798981-A-C

19393653-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68798981-A-T

19393654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68798982-G-A

19393654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68798982-G-T

19393667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68798991-G-A

19393667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68798991-G-T

19393670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68798994-T-C

http://identifiers.org/hco/8/GRCh38#19393683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68799007-C-A

19393683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68799007-C-T

http://identifiers.org/hco/8/GRCh38#19393684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68799008-C-A

19393684-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68799008-C-G

19393684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68799008-C-T

19393685-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68799009-T-A

19393685-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68799009-T-G

http://identifiers.org/hco/8/GRCh38#19393692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68799016-C-A

19393692-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68799016-C-G

19393692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68799016-C-T

19393763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68799079-G-A

19394387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68799161-T-C

http://identifiers.org/hco/8/GRCh38#19394439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68799203-C-A

http://identifiers.org/hco/8/GRCh38#19394445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68799209-C-A

19394445-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68799209-C-G

19394445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68799209-C-T

19394460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68799224-G-A

19394460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68799224-G-T

http://identifiers.org/hco/8/GRCh38#19394480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68799241-C-A

19394480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68799241-C-T

19394516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68799272-T-C

19394516-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68799272-T-G

http://identifiers.org/hco/8/GRCh38#19394558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68799314-C-A

19394558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 68799314-C-T

19394564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 68799320-T-C

19394645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 68799401-G-A

19394645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 68799401-G-T

19394649-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 68799405-C-G

19394649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 68799405-C-T

http://identifiers.org/hco/8/GRCh38#19394699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68799455-C-A

19394699-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 68799455-C-G

19394699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 68799455-C-T

19394779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 68799525-G-T

19394781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 68799527-G-A

19394781-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 68799527-G-C

19394781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 68799527-G-T

19394782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 68799528-T-C

19394782-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 68799528-T-G

19394854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 68799616-G-A

19394854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 68799616-G-T

http://identifiers.org/hco/8/GRCh38#19394861-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68799625-A-C

19394861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 68799625-A-G

http://identifiers.org/hco/8/GRCh38#19394904-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68799680-A-C

19394904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 68799680-A-G

19394943-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 68799722-A-T

19395118-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 68799898-C-G

19395118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 68799898-C-T

19395156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 68799936-C-T

19395185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 68799961-T-C

19395204-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 68800002-T-A

19395204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 68800002-T-C

19395391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 68800538-A-G

19395407-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 68800554-G-C

19395407-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 68800554-G-T

19395410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 68800557-G-A

19395446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 68800598-T-C

http://identifiers.org/hco/8/GRCh38#19395460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68800611-C-A

19395460-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 68800611-C-G

19395460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 68800611-C-T

http://identifiers.org/hco/8/GRCh38#19395470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68800621-C-A

19395470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 68800621-C-T

19395507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 68800658-G-T

19395518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 68800663-G-T

19395520-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 68800665-T-A

19395572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 68800705-G-A

19395572-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 68800705-G-C

19395582-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 68800715-G-C

19395601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 68800734-A-G

19395655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 68800786-G-A

19395663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 68800794-A-G

19395676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 68800803-A-G

http://identifiers.org/hco/8/GRCh38#19395765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68800895-C-A

19395812-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 68800927-T-G

19395822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 68800935-T-C

19395880-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 68800993-T-A

http://identifiers.org/hco/8/GRCh38#19395886-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68800999-A-C

http://identifiers.org/hco/8/GRCh38#19395926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68801040-C-A

http://identifiers.org/hco/8/GRCh38#19395982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68801095-C-A

19395982-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 68801095-C-G

19395986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 68801099-T-C

http://identifiers.org/hco/8/GRCh38#19396060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68801188-C-A

19396128-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 68801250-G-T

http://identifiers.org/hco/8/GRCh38#19396160-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#68801271-A-C

19396160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 68801271-A-G

19396180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26102
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 68801285-T-C