94574072-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 118349854-T-A

http://identifiers.org/hco/13/GRCh38#94574073-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118349855-A-C

94574073-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 118349855-A-T

94574285-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 118350072-T-A

http://identifiers.org/hco/13/GRCh38#94574466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118350229-C-A

94574482-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 118350245-T-A

94574482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 118350245-T-C

94574501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 118350264-G-A

94574575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 118350309-C-T

94574580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 118350314-A-G

http://identifiers.org/hco/13/GRCh38#94574605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118350338-C-A

94574605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 118350338-C-T

94574609-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 118350342-T-A

94574609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 118350342-T-C

94574670-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 118350391-A-T

94574672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 118350393-C-T

http://identifiers.org/hco/13/GRCh38#94574722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118350441-C-A

94574722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 118350441-C-T

http://identifiers.org/hco/13/GRCh38#94574724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118350443-C-A

94574727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 118350446-G-T

94574742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 118350463-C-T

94574744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 118350465-T-C

94574746-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 118350467-C-G

94574746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 118350467-C-T

http://identifiers.org/hco/13/GRCh38#94574758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118350478-C-A

94574758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 118350478-C-T

94574943-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118350646-T-G

http://identifiers.org/hco/13/GRCh38#94574952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118350655-C-A

94574952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118350655-C-T

94575159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118350800-G-A

94575209-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118350875-G-C

94575251-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118350919-T-A

http://identifiers.org/hco/13/GRCh38#94575260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118350928-C-A

94575260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118350928-C-T

94575264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118350932-G-A

94576143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118351568-A-G

94576181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118351595-T-C

94576257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118351665-T-C

94576302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118351713-T-C

94576415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 118351826-G-A

94576432-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118351840-T-A

94576432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118351840-T-C

94576449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118351855-T-C

94576543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118351941-C-T

94576655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118352042-A-G

http://identifiers.org/hco/13/GRCh38#94576672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118352059-C-A

94577290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118352456-T-C

94577291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118352457-G-A

94577291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118352457-G-T

94577304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118352468-T-C

94577306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118352470-T-C

94577312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118352473-A-G

94577321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118352482-A-G

http://identifiers.org/hco/13/GRCh38#94577326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118352487-C-A

94577326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118352487-C-T

94577332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118352495-T-C

94577332-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118352495-T-G

http://identifiers.org/hco/13/GRCh38#94577335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118352498-C-A

94577335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118352498-C-T

http://identifiers.org/hco/13/GRCh38#94577338-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118352502-A-C

94577338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118352502-A-G

94577338-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118352502-A-T

94577343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118352507-T-C

http://identifiers.org/hco/13/GRCh38#94577346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118352510-C-A

94577346-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118352510-C-G

94577346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118352510-C-T

http://identifiers.org/hco/13/GRCh38#94577359-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118352517-C-A

94577379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 118352537-A-G

94577383-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118352541-T-A

94577415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 118352573-A-G

94577415-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118352573-A-T

94577469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118352624-T-C

94577474-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118352629-T-G

http://identifiers.org/hco/13/GRCh38#94577519-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118352681-A-C

http://identifiers.org/hco/13/GRCh38#94577524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118352686-C-A

94577529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118352691-A-G

94577532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118352694-A-G

94578059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 118353545-G-A

http://identifiers.org/hco/13/GRCh38#94578158-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118353644-C-A

94578161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 118353647-A-G

94578202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118353688-G-T

http://identifiers.org/hco/13/GRCh38#94578247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118353716-C-A

94578247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118353716-C-T

94578257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118353726-G-T

94578358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118353821-G-T

94578390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118353864-G-A

http://identifiers.org/hco/13/GRCh38#94578606-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118354286-A-C

94578606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118354286-A-G

94578606-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118354286-A-T

http://identifiers.org/hco/13/GRCh38#94578613-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118354293-A-C

94578617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118354296-T-C

94578617-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118354296-T-G

94578756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118354408-T-C

94578866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118354510-A-G

94578886-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118354530-A-T

94579086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118354711-A-G

http://identifiers.org/hco/13/GRCh38#94579529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118354801-C-A

94579529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118354801-C-T

94579548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118354812-G-A

94579548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118354812-G-T

http://identifiers.org/hco/13/GRCh38#94579549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118354813-C-A

94579549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118354813-C-T

94579588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118354825-A-G

94579593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118354830-T-C

94579593-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118354830-T-G

94579677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118354946-G-A

94579678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118354947-G-A

94579678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118354947-G-T

94579697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118354971-G-A

94579697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118354971-G-T

http://identifiers.org/hco/13/GRCh38#94579733-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118354995-A-C

94579733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118354995-A-G

94579733-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118354995-A-T

94579779-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118355040-A-T

http://identifiers.org/hco/13/GRCh38#94579824-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118355084-A-C

94579825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118355085-A-G

94579873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118355128-G-A

94579873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118355128-G-T

http://identifiers.org/hco/13/GRCh38#94580000-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118355237-A-C

94580001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118355238-A-G

http://identifiers.org/hco/13/GRCh38#94580048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118355280-C-A

94580048-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118355280-C-G

94580048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118355280-C-T

94580072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118355312-G-A

94580285-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118356100-T-G

94580342-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118356158-G-C

94580520-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118356296-C-G

94580546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118356323-T-C

94580548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118356326-A-G

94580740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118356481-C-T

94581078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118357039-A-G

94581078-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118357039-A-T

94583067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118359107-G-A

94583067-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118359107-G-C

94583153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118359190-T-C

94583223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 118359260-T-C

http://identifiers.org/hco/13/GRCh38#94583274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118359311-C-A

94583274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118359311-C-T

94583337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118359368-T-C

94589618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118363689-T-C

94589686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118363752-C-T

94589900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118363897-T-C

94590041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118364038-T-C

94590137-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118364092-T-A

94590137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118364092-T-C

94590430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118364340-T-C

http://identifiers.org/hco/13/GRCh38#94590478-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118364388-A-C

94590724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118364655-G-T

http://identifiers.org/hco/13/GRCh38#94590744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118364682-C-A

94590771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118364794-T-C

94590817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118364871-C-T

94590846-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 118364900-T-A

94590846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 118364900-T-C

94590857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 118364911-A-G

94590881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 118364935-T-C

94590967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118365021-A-G

94590969-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118365023-G-C

http://identifiers.org/hco/13/GRCh38#94590993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118365044-C-A

94590993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118365044-C-T

94591055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118365110-G-T

94591118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118365171-G-A

94592155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118365549-C-T

http://identifiers.org/hco/13/GRCh38#94592162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118365556-C-A

94592162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118365556-C-T

94592220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118365611-G-A

94592220-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118365611-G-C

94592220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118365611-G-T

94592237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118365631-A-G

94592237-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118365631-A-T

94592329-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118365722-G-C

94592340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118365733-A-G

94593574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118367740-T-C

94593696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118367845-G-A

94593733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118367880-T-C

94593802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118367983-G-T

94593911-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 118368089-T-A

94593911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 118368089-T-C

94593941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118368118-A-G

94593994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118368169-A-G

94594556-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118368633-C-G

94594607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118368688-T-C

94594707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118368795-C-T

94594792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118368877-T-C

94594893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118368960-T-C

94594979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118369048-C-T

94595556-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118369521-A-T

http://identifiers.org/hco/13/GRCh38#94595675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118369663-C-A

94595675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118369663-C-T

94595679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118369680-T-C

94595754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118369739-G-A

94595754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118369739-G-T

http://identifiers.org/hco/13/GRCh38#94595831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118369814-C-A

94595831-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118369814-C-G

94595831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118369814-C-T

94595832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118369815-A-G

94595836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118369836-T-C

94595836-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118369836-T-G

http://identifiers.org/hco/13/GRCh38#94595953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118369956-C-A

94595953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118369956-C-T

94595994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 118369999-G-A

94595994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 118369999-G-T

94596112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 118370117-G-A

94596112-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 118370117-G-C

94596156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 118370159-T-C

94596159-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20324
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 118370162-T-G