14651831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91855120-A-G

14651890-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91855179-T-G

14651893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91855182-G-A

http://identifiers.org/hco/3/GRCh38#14651953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91855239-C-A

14651953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91855239-C-T

http://identifiers.org/hco/3/GRCh38#14651991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91855273-C-A

14651991-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91855273-C-G

14651991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91855273-C-T

14652164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91855431-C-T

http://identifiers.org/hco/3/GRCh38#14652253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91855493-C-A

14652380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91855619-G-A

14652521-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91855762-A-T

14653228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91856218-T-C

14653237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91856227-A-G

14653461-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91856467-C-G

14654302-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91857122-G-C

14654368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91857178-G-A

14654376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91857186-G-A

14654376-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91857186-G-C

http://identifiers.org/hco/3/GRCh38#14654623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91857426-C-A

14654740-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91857525-C-G

14655495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91858194-T-C

14655588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 91858287-T-C

14655657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91858332-G-A

14655657-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91858332-G-C

14655735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91858399-A-G

14655735-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91858399-A-T

http://identifiers.org/hco/3/GRCh38#14655737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91858401-C-A

14655737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91858401-C-T

http://identifiers.org/hco/3/GRCh38#14655738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91858402-C-A

14656167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91860277-A-G

http://identifiers.org/hco/3/GRCh38#14656218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91860331-C-A

14656218-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91860331-C-G

14656750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91860955-T-C

14658753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91862222-G-A

14658753-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91862222-G-C

14658753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91862222-G-T

14658761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91862230-G-A

14658761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91862230-G-T

http://identifiers.org/hco/3/GRCh38#14658839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91862298-C-A

14658839-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91862298-C-G

14658839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91862298-C-T

14658901-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 91862359-T-A

14658964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91862419-A-G

14658969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91862424-G-A

14659035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91862482-G-A

14659035-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91862482-G-C

14659035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91862482-G-T

14659200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91862601-G-A

14659210-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91862611-C-G

14659224-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91862624-G-C

14659809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91863529-T-C

14659809-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91863529-T-G

14660085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91863750-G-A

14660125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91863786-G-A

14660693-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91864265-C-G

14660792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91864359-A-G

14660837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91864396-G-A

14661193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91864738-A-G

14661209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91864757-G-A

14661209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91864757-G-T

14661329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91864857-G-A

14661381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91864926-G-A

14661381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91864926-G-T

14661395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91864936-A-G

14661422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91864962-G-T

http://identifiers.org/hco/3/GRCh38#14661429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91864969-C-A

14661429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91864969-C-T

http://identifiers.org/hco/3/GRCh38#14661437-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91864975-A-C

14661437-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91864975-A-T

14661442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91864980-G-A

14661442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91864980-G-T

http://identifiers.org/hco/3/GRCh38#14661443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91864981-C-A

14661443-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91864981-C-G

14661443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91864981-C-T

14661470-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91864984-T-G

http://identifiers.org/hco/3/GRCh38#14661479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91864993-C-A

14661479-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91864993-C-G

14661731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91865252-C-T

14661784-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91865305-T-G

http://identifiers.org/hco/3/GRCh38#14661794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91865316-C-A

14661794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91865316-C-T

14661797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91865319-T-C

14661797-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91865319-T-G

14661804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91865328-T-C

http://identifiers.org/hco/3/GRCh38#14661926-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91865437-A-C

14661950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91865461-G-A

14662090-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91865564-C-G

14662090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91865564-C-T

14662322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91865655-G-T

http://identifiers.org/hco/3/GRCh38#14662398-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91865702-A-C

14662402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91865706-G-A

14662619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91865861-T-C

http://identifiers.org/hco/3/GRCh38#14662825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91866007-C-A

14662825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91866007-C-T

14663006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91866145-C-T

14663414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91866261-A-G

14663483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91866325-G-A

14664039-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91866838-C-G

14664058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91866857-A-G

14664173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91866997-A-G

14664441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91867262-C-T

14664493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91867292-G-T

14664609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91867393-A-G

14664671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91867451-A-G

14664683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91867463-T-C

14664882-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91867650-T-G

http://identifiers.org/hco/3/GRCh38#14664895-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91867663-A-C

14664895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91867663-A-G

14665040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 91867787-G-A

14665130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 91867877-G-A

14665130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 91867877-G-T

14665191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91867926-G-A

http://identifiers.org/hco/3/GRCh38#14665197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91867932-C-A

14665197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91867932-C-T

14665207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91867942-A-G

14665269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91867989-T-C

14665397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91869038-C-T

http://identifiers.org/hco/3/GRCh38#14665625-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91869197-A-C

14665713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91869280-A-G

http://identifiers.org/hco/3/GRCh38#14666790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91869822-C-A

14666790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91869822-C-T

14666880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 91869912-G-A

14666892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 91869924-A-G

14666966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91870008-A-G

14666966-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91870008-A-T

14666976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91870018-A-G

14666993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91870037-A-G

14667001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91870044-G-A

14667015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91870058-G-A

http://identifiers.org/hco/3/GRCh38#14667101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91870125-C-A

14667101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91870125-C-T

http://identifiers.org/hco/3/GRCh38#14667123-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91870140-A-C

14667123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91870140-A-G

14667177-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91870194-T-A

14667177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91870194-T-C

14667182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91870199-A-G

http://identifiers.org/hco/3/GRCh38#14667323-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91870287-A-C

14667323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91870287-A-G

14667333-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91870297-T-G

14667334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91870298-G-A

14667369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 91870334-T-C

http://identifiers.org/hco/3/GRCh38#14667392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91870357-C-A

14667392-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91870357-C-G

http://identifiers.org/hco/3/GRCh38#14667417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91870380-C-A

http://identifiers.org/hco/3/GRCh38#14667552-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91870513-A-C

14667684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91871249-C-T

http://identifiers.org/hco/3/GRCh38#14667869-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91871838-A-C

14667869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91871838-A-G

14667885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91871852-G-A

14667885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91871852-G-T

14667901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91871868-G-T

14667911-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91871878-G-C

14667911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91871878-G-T

14667998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91872139-G-A

14667998-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91872139-G-C

14668013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91872154-G-A

http://identifiers.org/hco/3/GRCh38#14668015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91872156-C-A

14668191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91872337-G-A

http://identifiers.org/hco/3/GRCh38#14668219-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91872364-A-C

http://identifiers.org/hco/3/GRCh38#14668252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91872394-C-A

14668252-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91872394-C-G

14668252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91872394-C-T

http://identifiers.org/hco/3/GRCh38#14668271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91872404-C-A

14668271-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91872404-C-G

14668271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91872404-C-T

http://identifiers.org/hco/3/GRCh38#14668466-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91872748-A-C

14668466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91872748-A-G

14668548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91872811-A-G

14668576-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91872838-T-G

14668674-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91873865-C-G

14668674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91873865-C-T

14668770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91873953-A-G

14668915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91874060-T-C

14669019-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91874169-G-C

14669162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91874296-G-A

14669253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91874346-G-A

14669311-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91874422-C-G

14669311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91874422-C-T

14669526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91874615-G-A

14669589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91874672-C-T

http://identifiers.org/hco/3/GRCh38#14669591-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91874674-A-C

14669628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91874688-A-G

14669656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91874717-G-A

14669816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91875033-G-A

14669816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91875033-G-T

http://identifiers.org/hco/3/GRCh38#14669827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91875045-C-A

14669827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91875045-C-T

14669871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91875088-T-C

14669977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 91875171-G-T

http://identifiers.org/hco/3/GRCh38#14670025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91875219-C-A

14670025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 91875219-C-T

14670035-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 91875229-A-T

14670053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91875247-G-A

14670101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91875400-C-T

14670367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91875790-A-G

14670387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91875807-A-G

14670418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91875841-A-G

14670471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91875889-G-T

14670680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91876066-A-G

http://identifiers.org/hco/3/GRCh38#14670769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91876154-C-A

14670769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91876154-C-T

http://identifiers.org/hco/3/GRCh38#14670780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91876165-C-A

14670780-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91876165-C-G

14670780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91876165-C-T

14670795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91876179-G-A

http://identifiers.org/hco/3/GRCh38#14670848-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91876228-A-C

14670848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91876228-A-G

14670875-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91876254-T-A

14671021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91876398-T-C

14671021-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91876398-T-G

14671022-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91876399-G-C

14671056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 91876433-G-A

14671223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91876589-T-C

14671243-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91876596-C-G

14671243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91876596-C-T

14671265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91876610-T-C

http://identifiers.org/hco/3/GRCh38#14671282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91876630-C-A

14671282-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91876630-C-G

14671282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91876630-C-T

14671366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91876710-T-C

14671385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91876730-A-G

http://identifiers.org/hco/3/GRCh38#14671402-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91876876-A-C

http://identifiers.org/hco/3/GRCh38#14671493-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91877089-A-C

http://identifiers.org/hco/3/GRCh38#14671498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91877094-C-A

14671515-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91877111-T-G

14671578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91877174-G-A

14671578-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91877174-G-C

14671578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91877174-G-T

14671589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91877185-A-G

14671590-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91877186-G-C

14671590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91877186-G-T

14671595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91877191-G-A

14671595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91877191-G-T

http://identifiers.org/hco/3/GRCh38#14671604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91877200-C-A

14671604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91877200-C-T

14671615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91877207-G-A

14671615-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91877207-G-T

14671631-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91877223-T-A

14671631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91877223-T-C

http://identifiers.org/hco/3/GRCh38#14671649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91877255-C-A

14671649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91877255-C-T

http://identifiers.org/hco/3/GRCh38#14671715-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91877310-A-C

14671806-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91877384-T-A

14671806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91877384-T-C

14671806-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91877384-T-G

14671838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91877413-G-A

14671838-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91877413-G-C

14671838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91877413-G-T

14671841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91877416-G-A

14671845-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91877420-T-A

14671863-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91877438-T-G

14671885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91877459-A-G

http://identifiers.org/hco/3/GRCh38#14671924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91877499-C-A

14671924-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91877499-C-G

14671925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91877500-C-T

14671944-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91877518-A-T

http://identifiers.org/hco/3/GRCh38#14671947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91877521-C-A

14671947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91877521-C-T

14671976-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91877554-T-A

14672009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91877588-G-A

14672009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91877588-G-T

14672015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91877594-T-C

14672041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91877622-G-A

14672041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91877622-G-T

14672063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91877642-A-G

14672072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91877657-G-T

14672210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91877727-A-G

14672619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91878005-G-T

14672621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28033
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91878007-A-G