4562218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 126898775-G-A

4562218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 126898775-G-T

4562220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 126898773-A-G

4562303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 126898686-G-A

4562303-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 126898686-G-C

4562303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 126898686-G-T

http://identifiers.org/hco/12/GRCh38#4562340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126898664-C-A

4562340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 126898664-C-T

4562374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 126898639-A-G

4562534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 126898516-C-T

4562629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 126898447-C-T

http://identifiers.org/hco/12/GRCh38#4562770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126898376-C-A

4562860-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 126898270-T-A

4562860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 126898270-T-C

4562944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 126898210-G-T

http://identifiers.org/hco/12/GRCh38#4562987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126898172-C-A

4563238-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 126897878-G-C

4563302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 126897838-G-T

4563638-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 126897543-C-G

4563680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 126897522-T-C

4563691-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 126897511-G-C

4564048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 126897179-C-T

4564281-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 126897098-T-G

4564414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 126897050-C-T

http://identifiers.org/hco/12/GRCh38#4564439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126897028-C-A

http://identifiers.org/hco/12/GRCh38#4564440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126897027-C-A

4564465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 126897002-G-T

4564497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 126896969-A-G

4564497-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 126896969-A-T

4564581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 126896885-T-C

4564608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 126896856-T-C

4564684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 126896793-A-G

4564891-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 126896577-T-A

4564891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 126896577-T-C

4564929-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 126896536-C-G

4564969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 126896504-C-T

4564970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 126896503-G-A

4564970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 126896503-G-T

4565004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 126896467-C-T

4565010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 126896458-G-A

4565686-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 126895864-T-A

4565769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 126895829-G-A

4565808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 126895799-T-C

4566138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 126895553-G-A

4566138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 126895553-G-T

4566471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 126895235-G-A

4566504-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 126895203-G-C

4566504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 126895203-G-T

4566642-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 126895102-C-G

4566797-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 126894874-G-C

4567113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 126894405-A-G

4567278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 126894253-A-G

4567287-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 126894244-T-G

http://identifiers.org/hco/12/GRCh38#4567315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126894216-C-A

4567367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126894169-C-T

http://identifiers.org/hco/12/GRCh38#4567369-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126894167-A-C

4567500-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 126894044-T-A

4567500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 126894044-T-C

4567524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 126894020-G-A

4567524-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 126894020-G-C

4567525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 126894019-A-G

4567824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 126893679-C-T

http://identifiers.org/hco/12/GRCh38#4567927-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126893579-A-C

4568060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 126893235-T-C

http://identifiers.org/hco/12/GRCh38#4568068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126893227-C-A

4568069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 126893226-A-G

4568119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 126893175-G-A

4568119-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 126893175-G-C

4568119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 126893175-G-T

4571225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 126890098-A-G

4571229-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 126890094-G-C

http://identifiers.org/hco/12/GRCh38#4571674-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126889718-A-C

4571842-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 126889623-G-C

4571991-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 126889526-C-G

http://identifiers.org/hco/12/GRCh38#4572795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126887996-C-A

4572795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 126887996-C-T

4572870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126887945-G-A

4572870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126887945-G-T

http://identifiers.org/hco/12/GRCh38#4572937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126887877-C-A

4572952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126887862-T-C

4573101-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126887698-T-G

4573106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126887694-G-A

4573106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126887694-G-T

4573131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126887669-A-G

4573294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 126887532-G-A

4573347-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126887477-G-C

4573347-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126887477-G-T

4573364-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 126887460-C-G

4573364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 126887460-C-T

http://identifiers.org/hco/12/GRCh38#4573426-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126887398-A-C

4573451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 126887373-G-A

4573472-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 126887357-C-G

4573472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 126887357-C-T

4573852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 126887026-A-G

4580204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 126885110-A-G

4580360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 126884977-G-A

4580441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 126884896-C-T

4580794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 126884561-G-T

4580920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 126884342-G-T

4580951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 126884288-A-G

4580996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 126884243-C-T

http://identifiers.org/hco/12/GRCh38#4581018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126884221-C-A

4581018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 126884221-C-T

http://identifiers.org/hco/12/GRCh38#4581122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126884117-C-A

4586854-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 126878724-G-C

4586901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 126878669-A-G

4587032-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 126878467-C-G

4587044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 126878455-G-A

4587378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 126878171-C-T

4587757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 126877800-A-G

4588268-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 126877671-T-A

4588307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 126877633-G-A

4588680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 126877287-T-C

4588782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 126877067-T-C

http://identifiers.org/hco/12/GRCh38#4588814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126876973-C-A

4588814-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 126876973-C-G

4588814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 126876973-C-T

4588894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 126876884-A-G

4588928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 126876851-T-C

http://identifiers.org/hco/12/GRCh38#4589062-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126876715-A-C

4589885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 126876523-A-G

4589945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 126876365-A-G

4589978-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 126876341-T-A

http://identifiers.org/hco/12/GRCh38#4590053-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126876270-A-C

4590053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 126876270-A-G

4590053-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 126876270-A-T

http://identifiers.org/hco/12/GRCh38#4590056-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126876267-A-C

4590056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 126876267-A-G

4590106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 126876221-G-T

4590118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126876202-G-A

4590118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126876202-G-T

4590269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 126876077-A-G

4590281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 126876069-G-A

4590453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126875893-G-A

4590889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 126874526-G-T

4590899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 126874517-C-T

4591128-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 126874293-G-T

4591172-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126874250-C-G

4591347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126874075-G-A

4591347-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126874075-G-C

4591420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126874017-G-A

4591420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126874017-G-T

4591442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126873995-A-G

4591472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126873966-G-A

4591472-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126873966-G-C

4591472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126873966-G-T

4591507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126873911-G-A

4591507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126873911-G-T

4591540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126873878-T-C

4591540-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126873878-T-G

4591659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126873798-G-A

http://identifiers.org/hco/12/GRCh38#4591691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126873771-C-A

4591691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126873771-C-T

4591709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126873754-T-C

4592860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126871922-G-A

4592860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126871922-G-T

4592938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126871864-C-T

http://identifiers.org/hco/12/GRCh38#4592945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126871853-C-A

4592945-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126871853-C-G

4592945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126871853-C-T

4593190-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126871596-A-T

4593307-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126871459-A-T

4593317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126871452-A-G

4593656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126871105-G-A

4594709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126870451-C-T

http://identifiers.org/hco/12/GRCh38#4594978-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126870176-A-C

4595082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126870080-A-G

4595293-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126869901-C-G

4595293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126869901-C-T

4595591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126869599-G-A

4595664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126869529-G-A

4595664-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126869529-G-C

4595687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126869506-C-T

4595978-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126869333-C-G

4596475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126868863-G-A

4596475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126868863-G-T

4596505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126868834-G-T

4596893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126868450-A-G

4596999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126868340-T-C

4597074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126868269-T-C

4597077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126868266-G-A

4597077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126868266-G-T

4597195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron variant
orthologous variants: 126868152-G-A

4597195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron variant
orthologous variants: 126868152-G-T

4597213-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron variant
orthologous variants: 126868134-T-A

4597213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron variant
orthologous variants: 126868134-T-C

4597213-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron variant
orthologous variants: 126868134-T-G

http://identifiers.org/hco/12/GRCh38#4597223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126868124-C-A

http://identifiers.org/hco/12/GRCh38#4597227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126868120-C-A

4597227-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron variant
orthologous variants: 126868120-C-G

4597392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron variant
orthologous variants: 126868058-A-G

4597407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron variant
orthologous variants: 126868043-C-T

4597557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron variant
orthologous variants: 126867917-C-T

4598673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron variant
orthologous variants: 126867320-G-A

4598944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron variant
orthologous variants: 126867208-G-T

http://identifiers.org/hco/12/GRCh38#4598950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126867202-C-A

4598950-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron variant
orthologous variants: 126867202-C-G

4598950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron variant
orthologous variants: 126867202-C-T

http://identifiers.org/hco/12/GRCh38#4599065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126867086-C-A

4599174-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 126866977-C-G

4599174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 126866977-C-T

http://identifiers.org/hco/12/GRCh38#4599376-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126864075-C-A

4599401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron variant
orthologous variants: 126864050-G-A

http://identifiers.org/hco/12/GRCh38#4599532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126863908-C-A

4599571-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron variant
orthologous variants: 126863867-T-A

4599584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron variant
orthologous variants: 126863854-G-A

4599584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron variant
orthologous variants: 126863854-G-T

4599601-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron variant
orthologous variants: 126863837-G-C

4599601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron variant
orthologous variants: 126863837-G-T

4599606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron variant
orthologous variants: 126863832-T-C

http://identifiers.org/hco/12/GRCh38#4599649-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126863768-A-C

4599667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126863751-G-A

4599667-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126863751-G-C

4599667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126863751-G-T

http://identifiers.org/hco/12/GRCh38#4599882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126863522-C-A

4599882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126863522-C-T

4599921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126863485-G-A

4599921-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126863485-G-C

4599946-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126863468-T-G

http://identifiers.org/hco/12/GRCh38#4604909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126862367-C-A

4604909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 126862367-C-T

4604934-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126862342-C-G

4604934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126862342-C-T

4605027-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126862249-A-T

http://identifiers.org/hco/12/GRCh38#4605067-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126862209-A-C

4605067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126862209-A-G

4605103-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126862162-C-G

4605103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126862162-C-T

http://identifiers.org/hco/12/GRCh38#4605155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126862115-C-A

4605155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126862115-C-T

4605231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126862059-A-G

4605252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126862038-T-C

4606555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126861690-A-G

4606807-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126861500-C-G

4606831-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126861491-T-G

4606849-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126861476-C-G

4606954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126861373-T-C

4606957-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126861370-T-G

4606988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126861338-T-C

4606988-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126861338-T-G

4607177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126861197-G-T

4607213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126861165-A-G

http://identifiers.org/hco/12/GRCh38#4607289-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126861086-C-A

4607289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126861086-C-T

4607330-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126861045-C-G

4607330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 126861045-C-T

4607396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126860979-T-C

4607455-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126860873-T-A

4607472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126860857-G-A

4607472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126860857-G-T

4607606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126860753-C-T

4608610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126859633-T-C

4608754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126859522-A-G

http://identifiers.org/hco/12/GRCh38#4608884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126859407-C-A

4608963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126859338-A-G

4609092-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126859166-T-G

4609296-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126859009-G-C

4609904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126857588-G-A

4609922-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126857570-A-T

4609956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126857538-A-G

4609971-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126857523-T-A

4609971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126857523-T-C

4609971-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126857523-T-G

4610027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126857462-G-T

http://identifiers.org/hco/12/GRCh38#4610063-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126857426-A-C

4610063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126857426-A-G

4610086-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126857403-A-T

4610204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 126857266-A-G

4610244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126857226-T-C

4610340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126857126-A-G

4610394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126857071-G-T

4610422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126857035-T-C

4610448-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126857024-T-A

http://identifiers.org/hco/12/GRCh38#4610449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126857023-C-A

4610505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126857020-G-A

4610505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126857020-G-T

4610513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126857012-G-A

4610513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126857012-G-T

4610572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126856995-G-T

http://identifiers.org/hco/12/GRCh38#4610596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126856971-C-A

4610596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126856971-C-T

http://identifiers.org/hco/12/GRCh38#4610604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126856963-C-A

4610604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126856963-C-T

4610653-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126856917-G-C

4610653-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126856917-G-T

4610671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126856898-T-C

4610672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126856897-G-A

4610825-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126856750-T-G

4611426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126856129-G-A

4611608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126855934-A-G

4611642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126855900-T-C

4612386-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126854452-T-G

4612448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126854398-A-G

http://identifiers.org/hco/12/GRCh38#4612509-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126854335-A-C

4612568-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126854274-C-G

4612942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126854043-G-A

4613271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126853723-C-T

4613401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126853609-T-C

4613401-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126853609-T-G

4613458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126853569-T-C

4613505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 126853521-C-T

http://identifiers.org/hco/12/GRCh38#4613547-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126853479-A-C

4613625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 126853401-C-T

4613653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126853373-A-G

4613715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126853320-T-C

4613920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: 3 prime UTR variant
orthologous variants: 126853099-A-G

4613936-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: 3 prime UTR variant
orthologous variants: 126853086-T-A

4613936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: 3 prime UTR variant
orthologous variants: 126853086-T-C

4613965-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: 3 prime UTR variant
orthologous variants: 126853053-T-A

4613965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: 3 prime UTR variant
orthologous variants: 126853053-T-C

4613968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: 3 prime UTR variant
orthologous variants: 126853050-A-G

4613968-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: 3 prime UTR variant
orthologous variants: 126853050-A-T

4613981-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: 3 prime UTR variant
orthologous variants: 126853036-T-A

4613981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: 3 prime UTR variant
orthologous variants: 126853036-T-C

4613985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: 3 prime UTR variant
orthologous variants: 126853032-G-T

4613998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: 3 prime UTR variant
orthologous variants: 126853026-T-C

http://identifiers.org/hco/12/GRCh38#4614017-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126853007-C-A

4614017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: 3 prime UTR variant
orthologous variants: 126853007-C-T

4614066-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: 3 prime UTR variant
orthologous variants: 126852962-T-A

4614071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: 3 prime UTR variant
orthologous variants: 126852953-G-A

4614071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3095
most severe consequence: 3 prime UTR variant
orthologous variants: 126852953-G-T