49014239-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32663991-A-T

49014334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32663896-C-T

http://identifiers.org/hco/10/GRCh38#49014408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32663814-C-A

49014408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32663814-C-T

http://identifiers.org/hco/10/GRCh38#49014455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32663783-C-A

49014458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32663780-G-A

49014459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32663779-G-T

49014597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32663666-G-T

49014711-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32663558-T-A

49014711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32663558-T-C

49014711-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32663558-T-G

49014749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32663527-A-G

49014750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32663525-G-T

49014783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32663498-G-A

49014783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32663498-G-T

49014784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32663497-T-C

49014800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32663480-C-T

49014826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32663457-T-C

49014838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32663445-G-A

49014838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32663445-G-T

http://identifiers.org/hco/10/GRCh38#49014839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32663444-C-A

49014839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32663444-C-T

49014881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32663403-T-C

http://identifiers.org/hco/10/GRCh38#49014883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32663401-C-A

49014883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32663401-C-T

49014887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32663397-A-G

49014945-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32663354-T-A

49014945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32663354-T-C

49015018-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32663277-T-A

49015023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32663274-G-T

49015048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32663249-G-T

http://identifiers.org/hco/10/GRCh38#49015089-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32663205-C-A

49015089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32663205-C-T

49015090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32663204-T-C

http://identifiers.org/hco/10/GRCh38#49015671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32662934-C-A

49015671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32662934-C-T

http://identifiers.org/hco/10/GRCh38#49015710-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32662892-C-A

49015788-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32662821-T-A

49015799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32662810-C-T

49015830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32662779-T-C

49016016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32662526-G-A

49016016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32662526-G-T

49016029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32662513-G-A

49016029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32662513-G-T

http://identifiers.org/hco/10/GRCh38#49016099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32662437-C-A

49016099-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32662437-C-G

49016302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32662201-T-C

49016302-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32662201-T-G

49016312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32662182-G-T

49016401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32661974-G-A

49016401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32661974-G-T

49016475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32661867-T-C

49016499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32661834-A-G

49016518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32661815-C-T

http://identifiers.org/hco/10/GRCh38#49016659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32661747-C-A

49016684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32661728-G-A

http://identifiers.org/hco/10/GRCh38#49016701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32661711-C-A

49016741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32661677-G-A

49016749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32661669-C-T

49016786-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32661634-T-A

49016805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32661615-G-T

http://identifiers.org/hco/10/GRCh38#49016814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32661607-C-A

49016814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32661607-C-T

49016815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32661606-G-A

49016815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32661606-G-T

49016848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32661575-G-A

49016848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32661575-G-T

http://identifiers.org/hco/10/GRCh38#49016944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32661475-C-A

49016977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32661444-G-T

49017068-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32661349-T-G

49017123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32661308-T-C

49017153-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32661278-C-G

49017153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32661278-C-T

49017200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32661230-T-C

49017274-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32661166-A-T

49017306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32661134-G-A

49017346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32661096-A-G

49018505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32660900-T-C

49018587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32660823-C-T

49018609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32660812-A-G

49018612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32660809-C-T

49018642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32660777-A-G

http://identifiers.org/hco/10/GRCh38#49018661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32660742-C-A

49018704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32660699-A-G

http://identifiers.org/hco/10/GRCh38#49018805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32660601-C-A

49018805-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32660601-C-G

49018805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32660601-C-T

49018810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32660596-A-G

http://identifiers.org/hco/10/GRCh38#49018840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32660568-C-A

49018840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32660568-C-T

49018911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32660508-G-T

49019010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32660432-G-A

http://identifiers.org/hco/10/GRCh38#49019095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32660340-C-A

49019180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32660250-G-A

49019180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32660250-G-T

49019215-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32660212-T-A

49019356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32660076-G-T

49019415-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32660032-A-T

http://identifiers.org/hco/10/GRCh38#49019419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32660028-C-A

49019419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32660028-C-T

49019496-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32659960-T-A

49019496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32659960-T-C

49019518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32659939-A-G

49019555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32659903-A-G

49019611-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32659848-T-A

49019611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32659848-T-C

49019621-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32659846-T-G

http://identifiers.org/hco/10/GRCh38#49019623-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32659844-A-C

49019624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32659843-A-G

49019635-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32659832-G-C

http://identifiers.org/hco/10/GRCh38#49019794-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32659671-A-C

49020409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32658675-A-G

http://identifiers.org/hco/10/GRCh38#49020443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32658636-C-A

49020443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32658636-C-T

49020513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32658561-A-G

49020550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32658522-G-A

49020550-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32658522-G-C

49020578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32658495-G-A

http://identifiers.org/hco/10/GRCh38#49020708-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32658375-A-C

49020877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32658160-T-C

49021036-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32658008-T-A

49021853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32657529-G-A

49021964-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32657446-C-G

49022183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32657265-G-A

49022186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32657262-A-G

49022268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32657178-G-T

49022482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32656984-T-C

49022514-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32656952-C-G

49022514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32656952-C-T

49022535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32656939-C-T

49022574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32656899-G-A

49023512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32655966-T-C

http://identifiers.org/hco/10/GRCh38#49023576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32655893-C-A

49027967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32654801-A-G

49028217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32654573-T-C

49028728-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32654086-C-G

49029091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32653735-C-T

49029251-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32653587-T-G

49029407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32653418-T-C

http://identifiers.org/hco/10/GRCh38#49029950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32652716-C-A

49029954-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32652712-T-G

49030057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32652603-C-T

49030397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32652276-G-A

49030659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32652017-C-T

http://identifiers.org/hco/10/GRCh38#49030811-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32651856-A-C

http://identifiers.org/hco/10/GRCh38#49030995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32651677-C-A

49030995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32651677-C-T

49031074-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32651602-T-G

49031096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32651583-T-C

49031200-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32651510-C-G

49031331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32651362-T-C

49032112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32650802-G-A

49032154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32650767-A-G

49032387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32650375-G-A

49032387-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32650375-G-C

49032840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32649781-A-G

49032954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32649653-G-T

49033242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32649397-G-A

49033406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32649240-G-A

49033406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32649240-G-T

49033600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32649040-G-T

49033613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32649033-C-T

49033807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32648877-G-T

49033913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32648773-A-G

49033952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32648743-A-G

49033954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32648741-T-C

49033960-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32648735-T-G

49033969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32648726-C-T

http://identifiers.org/hco/10/GRCh38#49033978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32648720-C-A

49033978-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32648720-C-G

49033978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32648720-C-T

49033986-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32648712-T-A

49034005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32648693-C-T

49034123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32648596-A-G

49034128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32648591-C-T

49034678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32648000-T-C

49035029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32647680-G-T

49035153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32647558-G-T

49035497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32647266-A-G

49035926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32647028-T-C

49035952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32647002-C-T

49036051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32646939-A-G

49036137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 32646865-C-T

49036138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 32646864-G-A

49036325-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32646676-G-C

49039251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32645858-T-C

49040657-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32644561-T-G

49040817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32644370-T-C

49040995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32644118-C-T

49040999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32644114-A-G

49041107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32643925-A-G

http://identifiers.org/hco/10/GRCh38#49041128-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32643904-A-C

49046889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32641333-T-C

http://identifiers.org/hco/10/GRCh38#49047038-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32641195-A-C

49047038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32641195-A-G

49047136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32641096-T-C

49047191-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32641044-T-G

http://identifiers.org/hco/10/GRCh38#49047214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32641020-C-A

49047335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32640916-G-A

49047389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32640872-G-A

http://identifiers.org/hco/10/GRCh38#49047709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32640599-C-A

http://identifiers.org/hco/10/GRCh38#49047819-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32640504-A-C

49047920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32640391-T-C

49048382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32639992-G-A

49048382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32639992-G-T

49048434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32639939-A-G

49048526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32639848-T-C

49048636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32639739-A-G

49048636-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32639739-A-T

49048710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32639669-G-A

49048710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32639669-G-T

http://identifiers.org/hco/10/GRCh38#49048715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32639664-C-A

49048715-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32639664-C-G

49048715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32639664-C-T

49048729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32639650-G-A

49048729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32639650-G-T

http://identifiers.org/hco/10/GRCh38#49048855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32639529-C-A

49048882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32639502-T-C

49048893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32639491-G-A

49049003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32639371-C-T

49049088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32639285-G-A

http://identifiers.org/hco/10/GRCh38#49049211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32639185-C-A

49049404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32638739-T-C

49049650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32638423-G-A

49049650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32638423-G-T

49049833-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32638274-G-C

49050127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32637996-T-C

49050401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32637731-A-G

49050536-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32637609-T-G

49050785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32637371-G-A

49050785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32637371-G-T

49050796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32637360-C-T

49050986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32637156-C-T

49051013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32637121-T-C

49051015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32637119-G-A

49051266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32636900-G-A

49051266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32636900-G-T

49051267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32636899-T-C

49051268-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32636898-C-G

49051298-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32636868-T-G

49051378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32636744-G-T

49051403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32636711-T-C

http://identifiers.org/hco/10/GRCh38#49051409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32636705-C-A

49051409-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32636705-C-G

49051409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32636705-C-T

49051410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32636704-T-C

49051416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32636698-G-A

49051416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32636698-G-T

49051422-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32636692-G-C

49051422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32636692-G-T

http://identifiers.org/hco/10/GRCh38#49052386-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32635794-A-C

49052696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32635321-T-C

49052696-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32635321-T-G

49052723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32635297-C-T

49053002-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32635021-T-A

49053002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32635021-T-C

49053479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32634555-C-T

49053562-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32634470-G-C

49053804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32633960-C-T

49054079-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32633681-G-C

49054207-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32633567-A-T

49054585-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32633244-T-G

49055085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32632810-T-C

49055399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32632535-T-C

49055454-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32632486-T-A

49055513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32632429-A-G

49055569-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32632373-C-G

49055900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32632068-C-T

49056128-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32631842-T-G

49056160-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32631812-A-T

49056197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32631774-T-C

49056309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32631656-C-T

49058780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32630848-C-T

49058837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32630802-T-C

49058855-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32630781-C-G

49059083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32630613-C-T

http://identifiers.org/hco/10/GRCh38#49059244-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32630469-A-C

49059461-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32629606-C-G

49059507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32629549-T-C

49059605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32629459-G-A

49059795-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32629256-T-G

49059851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32629183-G-A

49060044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32628998-C-T

49060064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32628983-A-G

49060071-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32628976-T-A

49060071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32628976-T-C

49060457-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32628595-A-T

49060731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32628330-T-C

49061001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32628038-C-T

49061387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32627711-A-G

49062079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32627073-A-G

49064410-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32626858-T-A

49064413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32626855-G-A

49064413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32626855-G-T

49064441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32626839-G-A

http://identifiers.org/hco/10/GRCh38#49064447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32626833-C-A

49064447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32626833-C-T

http://identifiers.org/hco/10/GRCh38#49064459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32626826-C-A

49064459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32626826-C-T

49064462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32626823-C-T

49064464-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32626821-T-A

http://identifiers.org/hco/10/GRCh38#49064465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32626820-C-A

49064465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32626820-C-T

49064466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32626819-C-T

49064490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32626758-A-G

http://identifiers.org/hco/10/GRCh38#49064511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32626736-C-A

49064511-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32626736-C-G

49064511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32626736-C-T

49064514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32626733-G-A

49064514-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32626733-G-C

49064514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32626733-G-T

49064626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32626628-A-G

49064642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32626612-T-C

http://identifiers.org/hco/10/GRCh38#49064679-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32626575-A-C

49064835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32626436-A-G

49065344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32625792-G-A

49065356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32625781-G-T

49065870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32625296-T-C

49066295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32624912-T-C

49066392-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32624821-A-T

49066885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32624282-A-G

49066915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32624267-A-G

49067060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32624124-T-C

http://identifiers.org/hco/10/GRCh38#49067120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32624077-C-A

49067220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32623957-T-C

http://identifiers.org/hco/10/GRCh38#49067763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32623434-C-A

http://identifiers.org/hco/10/GRCh38#49067885-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32623371-A-C

49067886-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32623370-A-T

49068246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32623276-C-T

49068310-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32623214-G-T

49068530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32623019-T-C

49068560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32622987-A-G

49069189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32622431-C-T

http://identifiers.org/hco/10/GRCh38#49069260-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32622354-A-C

49070596-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32621397-A-T

49070713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32621256-C-T

49070768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32621175-T-C

49070939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32621003-G-A

http://identifiers.org/hco/10/GRCh38#49070944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32620998-C-A

49070944-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32620998-C-G

49071212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32619417-G-A

49071212-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32619417-G-C

49071302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32619324-T-C

49071430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32619192-C-T

49071449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32619173-A-G

49071535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32619084-G-T

49071784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32618913-A-G

49071880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32618828-C-T

49072143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32618582-A-G

49073399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32618366-T-C

49073443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32618324-G-A

49073581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32618210-T-C

49073610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32618169-A-G

49073647-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32618147-C-G

49073647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32618147-C-T

49074046-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32617768-C-G

49074062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32617752-C-T

49075025-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32617036-C-G

49075046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32617015-C-T

49075124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32616952-C-T

49075183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32616886-G-A

49075201-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32616873-C-G

49075201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32616873-C-T

49075249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32616828-T-C

49075306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32616785-C-T

49075318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32616773-G-A

49075606-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32616463-T-G

49075769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32616329-C-T

49075812-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32616285-T-A

49075827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32616270-G-A

49075922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32615989-A-G

49075939-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32615969-T-A

49076143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32615751-C-T

49076249-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32615655-G-C

49076420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32615524-A-G

49076423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32615519-G-T

49076441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32615501-G-T

49076632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32615226-C-T

49076931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32614993-T-C

49077116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32614788-A-G

49077116-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32614788-A-T

49077281-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32614626-C-G

49077281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32614626-C-T

49077302-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32614605-A-T

49077311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32614596-G-A

49077337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32614570-A-G

49080727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32613459-A-G

49080735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32613451-C-T

49080751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32613432-A-G

49080871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32613334-G-A

49081145-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32613088-A-T

49081147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32613084-C-T

49081192-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32613040-G-C

49081496-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32612750-G-C

49081685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32612593-C-T

49081731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32612549-C-T

http://identifiers.org/hco/10/GRCh38#49081797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32612483-C-A

49081797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32612483-C-T

49081894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32612392-C-T

49082137-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32612175-C-G

http://identifiers.org/hco/10/GRCh38#49082428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32611906-C-A

49082453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32611898-C-T

49082597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32611786-C-T

49082611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32611772-G-A

49082684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32611722-G-A

49082925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32611482-G-T

49083073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32611345-A-G

49083237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32611157-G-A

49083426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32610968-T-C

49084043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32610747-C-T

49084061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32610729-C-T

49084270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32610529-C-T

49084765-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32609928-G-C

49084848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32609847-G-A

49084873-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32609830-T-A

49084873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32609830-T-C

49084873-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32609830-T-G

49084955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32609763-G-T

49085461-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32609275-T-G

49085463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32609273-A-G

http://identifiers.org/hco/10/GRCh38#49085493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32609243-C-A

49085947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 32608985-A-G

http://identifiers.org/hco/10/GRCh38#49086047-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32608887-A-C

49086047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32608887-A-G

49086080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32608815-T-C

http://identifiers.org/hco/10/GRCh38#49086303-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32608598-A-C

49086387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32608528-C-T

49086515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32608400-T-C

49086558-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32608361-A-T

49086790-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32608208-T-G

49087030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32607822-A-G

49087108-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32607745-T-G

49087116-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32607737-G-C

49087228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32607646-G-T

49087321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32607555-C-T

49087482-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32607395-T-A

49087731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32607164-A-G

http://identifiers.org/hco/10/GRCh38#49088396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32606450-C-A

49088396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32606450-C-T

http://identifiers.org/hco/10/GRCh38#49088468-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32606370-A-C

49088625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32606211-G-A

http://identifiers.org/hco/10/GRCh38#49088652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32606187-C-A

49088652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32606187-C-T

49088755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32606080-C-T

49088757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32606078-T-C

49088851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32605984-T-C

49088984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32605854-T-C

49089192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32604627-G-A

49089230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32604571-G-A

49089344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32604460-T-C

49089446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32604314-C-T

49089655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32604132-G-A

49089777-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32604008-A-T

49089781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32604004-A-G

49090078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32603705-T-C

http://identifiers.org/hco/10/GRCh38#49090356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32603508-C-A

49090356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32603508-C-T

http://identifiers.org/hco/10/GRCh38#49090990-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32603108-A-C

http://identifiers.org/hco/10/GRCh38#49091043-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32603068-A-C

49091048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32603063-A-G

http://identifiers.org/hco/10/GRCh38#49091519-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32602601-A-C

49092126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32602176-C-T

49092258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32602051-G-A

49092284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32602025-T-C

http://identifiers.org/hco/10/GRCh38#49093742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32600928-C-A

49093742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32600928-C-T

http://identifiers.org/hco/10/GRCh38#49094173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32600329-C-A

49094173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32600329-C-T

49094343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32600188-A-G

49094496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32600078-A-G

http://identifiers.org/hco/10/GRCh38#49094996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32599655-C-A

http://identifiers.org/hco/10/GRCh38#49095055-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32599595-A-C

49095314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32599383-A-G

49095427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32599265-G-A

49095537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32599089-A-G

49095686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32598962-C-T

49095802-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32598888-C-G

49095818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32598872-A-G

49097377-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32597294-T-G

49097423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32597249-T-C

49097512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32597137-G-A

49097824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32595271-A-G

49097862-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32595185-G-C

49097877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32595173-C-T

49097888-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32595162-T-G

49098012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32595043-C-T

49098555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32594307-C-T

49098702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32594005-A-G

49098994-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32593407-C-G

49099009-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32593388-T-A

49099009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32593388-T-C

49099013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32593384-G-A

49099347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32593067-G-A

49099619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32592797-A-G

49100096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32591399-A-G

49100326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32591203-C-T

49100365-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32591166-C-G

49100627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32590867-G-A

49100652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32590842-A-G

http://identifiers.org/hco/10/GRCh38#49105950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32587665-C-A

http://identifiers.org/hco/10/GRCh38#49106222-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32587414-A-C

49106325-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32587312-A-T

49106654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32587116-A-G

49106713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32587059-A-G

49106891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32586890-T-C

49107372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32586110-C-T

49107448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32586040-T-C

49107456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32586030-G-A

49107456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32586030-G-T

49107481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32586006-G-A

49107481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32586006-G-T

49107501-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32585982-A-T

49107544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32585937-T-C

49107546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32585935-C-T

49107577-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32585906-G-C

http://identifiers.org/hco/10/GRCh38#49107587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32585896-C-A

49107605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32585875-G-A

49107608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32585872-G-A

49107696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32585784-G-T

49107764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32585716-C-T

49107833-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32585647-G-C

49107947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32585536-T-C

49108027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32585456-G-A

49108027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32585456-G-T

49108054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32585429-G-A

49108054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32585429-G-T

49108074-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32585410-G-C

49108074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32585410-G-T

49108271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32585054-A-G

49108394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32584968-C-T

49108436-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32584943-G-C

49108792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32584558-G-T

49108933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32584445-C-T

49108949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32584429-G-A

49109408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32584110-C-T

49109485-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32584049-A-T

49109545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32583996-T-C

49109879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32583566-C-T

49110360-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32583103-T-A

49110360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32583103-T-C

49110394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32583046-A-G

49110731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32582745-G-T

http://identifiers.org/hco/10/GRCh38#49110883-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32582605-A-C

http://identifiers.org/hco/10/GRCh38#49110887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32582601-C-A

http://identifiers.org/hco/10/GRCh38#49110937-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32582548-A-C

49110963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32582483-G-A

49111167-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32582285-G-C

49111337-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32582118-A-T

49111396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32582057-C-T

49111488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32581973-C-T

49111661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32581828-C-T

49111817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32581710-T-C

49111995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32581499-G-A

49112021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32581475-G-A

http://identifiers.org/hco/10/GRCh38#49112242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32581260-C-A

49112242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32581260-C-T

49112357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32581140-A-G

49112455-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32581022-C-G

49112547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32580946-A-G

49112634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32580866-G-A

49112872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32580643-T-C

http://identifiers.org/hco/10/GRCh38#49113035-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32580506-A-C

49113035-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32580506-A-T

49113040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32580503-C-T

49113089-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32580447-A-T

http://identifiers.org/hco/10/GRCh38#49113363-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32580271-A-C

49113545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32580072-G-T

49113567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32580050-G-A

49113591-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32580026-G-C

49114547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32579652-C-T

49114588-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32579611-T-G

49114681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32579513-G-A

49114951-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32579319-T-A

49115004-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32579270-T-G

http://identifiers.org/hco/10/GRCh38#49115099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32579188-C-A

http://identifiers.org/hco/10/GRCh38#49115418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32578934-C-A

49115418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32578934-C-T

http://identifiers.org/hco/10/GRCh38#49115506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32578843-C-A

49115506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26470
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32578843-C-T