186191573-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: 5 prime UTR variant
orthologous variants: 45786326-T-G

186191574-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: 5 prime UTR variant
orthologous variants: 45786325-T-A

http://identifiers.org/hco/4/GRCh38#186191590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45786305-C-A

186191590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: 5 prime UTR variant
orthologous variants: 45786305-C-T

186191598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: 5 prime UTR variant
orthologous variants: 45786297-C-T

186191600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: 5 prime UTR variant
orthologous variants: 45786295-G-A

186191628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 45786267-A-G

186191628-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 45786267-A-T

186191640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 45786255-G-A

186191640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 45786255-G-T

186191653-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: 5 prime UTR variant
orthologous variants: 45786242-T-A

186191653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: 5 prime UTR variant
orthologous variants: 45786242-T-C

186191653-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: 5 prime UTR variant
orthologous variants: 45786242-T-G

186191686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: 5 prime UTR variant
orthologous variants: 45786216-G-A

186191686-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: 5 prime UTR variant
orthologous variants: 45786216-G-C

186191686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: 5 prime UTR variant
orthologous variants: 45786216-G-T

186191724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: 5 prime UTR variant
orthologous variants: 45786122-G-A

186191724-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: 5 prime UTR variant
orthologous variants: 45786122-G-C

186191724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: 5 prime UTR variant
orthologous variants: 45786122-G-T

186191729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: 5 prime UTR variant
orthologous variants: 45786117-G-A

186191731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: 5 prime UTR variant
orthologous variants: 45786115-G-A

186191731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: 5 prime UTR variant
orthologous variants: 45786115-G-T

186191766-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 45786075-C-G

http://identifiers.org/hco/4/GRCh38#186191799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45786042-C-A

186191799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: 5 prime UTR variant
orthologous variants: 45786042-C-T

http://identifiers.org/hco/4/GRCh38#186191813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45786024-C-A

186191813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: 5 prime UTR variant
orthologous variants: 45786024-C-T

http://identifiers.org/hco/4/GRCh38#186191886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45785951-C-A

186191886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: synonymous variant
orthologous variants: 45785951-C-T

186192308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron variant
orthologous variants: 45785586-C-T

http://identifiers.org/hco/4/GRCh38#186193358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45782924-C-A

http://identifiers.org/hco/4/GRCh38#186193478-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45782819-A-C

186193652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 45782650-T-C

186193652-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 45782650-T-G

186193907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 45782405-T-C

186193908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 45782404-C-T

http://identifiers.org/hco/4/GRCh38#186194062-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45782250-A-C

186194076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 45781691-A-G

186194119-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 45781631-C-G

186194119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 45781631-C-T

186194150-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 45781600-C-G

186194150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 45781600-C-T

186194154-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 45781599-C-G

186194154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 45781599-C-T

186194161-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 45781592-A-T

186194164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 45781589-C-T

186194171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 45781582-C-T

186194198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 45781554-G-A

186194255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 45781502-C-T

186194337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 45781420-G-A

http://identifiers.org/hco/4/GRCh38#186194355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45781402-C-A

186194356-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 45781401-A-T

http://identifiers.org/hco/4/GRCh38#186194416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45781345-C-A

186194435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 45781326-T-C

186194438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 45781323-G-A

186194438-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 45781323-G-C

186194619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 45781140-A-G

186194619-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 45781140-A-T

http://identifiers.org/hco/4/GRCh38#186194656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45781110-C-A

186194656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron variant
orthologous variants: 45781110-C-T

http://identifiers.org/hco/4/GRCh38#186194671-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45781095-A-C

186194695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron variant
orthologous variants: 45781062-T-C

186194760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron variant
orthologous variants: 45781007-T-C

186194782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron variant
orthologous variants: 45780980-G-A

186194782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron variant
orthologous variants: 45780980-G-T

186194803-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron variant
orthologous variants: 45780961-C-G

186195988-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron variant
orthologous variants: 45774847-T-G

186196127-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45774701-G-C

186196127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45774701-G-T

186196212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45774581-A-G

186196217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45774576-G-A

186196217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45774576-G-T

186196515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45774122-A-G

186196581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45774055-G-T

186196692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45773955-G-T

186196802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45773848-G-T

186196842-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45773827-T-G

http://identifiers.org/hco/4/GRCh38#186196861-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45773807-A-C

186197137-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 45773555-C-G

186197163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45773541-G-T

http://identifiers.org/hco/4/GRCh38#186197213-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45773491-A-C

186197213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45773491-A-G

186197248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45773452-G-T

186197264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45773438-G-A

186197264-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45773438-G-C

186197264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45773438-G-T

http://identifiers.org/hco/4/GRCh38#186197265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45773437-C-A

186197302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45773399-T-C

186197323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45773378-G-A

186197323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45773378-G-T

http://identifiers.org/hco/4/GRCh38#186197352-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45773346-A-C

186197352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45773346-A-G

186197457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45773267-G-A

186197457-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45773267-G-C

186197501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45773227-T-C

186197578-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45773150-C-G

186197796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45772902-A-G

186197965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45772549-T-C

186198028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45772489-T-C

186198084-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45772411-C-G

186198281-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45772238-C-G

186198309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45772216-A-G

http://identifiers.org/hco/4/GRCh38#186198429-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45771490-A-C

186198564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45771282-G-A

186198758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45771015-C-T

186198870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45770903-G-A

186198924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45770856-A-G

http://identifiers.org/hco/4/GRCh38#186199589-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45770259-A-C

186199679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45770175-A-G

186200334-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45769526-C-G

186200587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45769323-C-T

http://identifiers.org/hco/4/GRCh38#186200815-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45769089-A-C

186200815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45769089-A-G

186201010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45768894-A-G

186201029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45768875-T-C

186201029-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45768875-T-G

186201056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45768853-A-G

http://identifiers.org/hco/4/GRCh38#186201062-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45768845-A-C

http://identifiers.org/hco/4/GRCh38#186201075-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45768822-A-C

186201202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45768710-A-G

186201424-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45767187-T-A

186201424-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45767187-T-G

http://identifiers.org/hco/4/GRCh38#186201492-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45767130-A-C

http://identifiers.org/hco/4/GRCh38#186201494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45767128-C-A

186201494-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45767128-C-G

http://identifiers.org/hco/4/GRCh38#186201573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45767100-C-A

186201573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45767100-C-T

186201592-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45767081-T-A

186201597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45767076-G-T

186201648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45767025-G-A

186201648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45767025-G-T

186201649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45767024-G-A

186201649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45767024-G-T

186201654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45767019-A-G

http://identifiers.org/hco/4/GRCh38#186201819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45766899-C-A

http://identifiers.org/hco/4/GRCh38#186201824-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45766894-C-A

http://identifiers.org/hco/4/GRCh38#186201897-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45766817-C-A

186201897-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45766817-C-G

186201897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45766817-C-T

186201961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45766756-G-A

http://identifiers.org/hco/4/GRCh38#186201986-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#45766730-A-C

186202019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45766694-C-T

186204529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 45764091-T-C

186204593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 45764046-A-G

186204593-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 45764046-A-T

186204641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45764007-A-G

186204736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45763920-A-G

http://identifiers.org/hco/4/GRCh38#186204793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45763863-C-A

186204793-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45763863-C-G

186204793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45763863-C-T

186204801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45763855-G-T

186204833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45763823-G-T

186205061-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45763446-G-C

186205068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45763439-A-G

186205081-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45763426-T-A

186205088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45763422-G-A

186205088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45763422-G-T

http://identifiers.org/hco/4/GRCh38#186205119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45763391-C-A

186205119-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45763391-C-G

http://identifiers.org/hco/4/GRCh38#186205124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45763386-C-A

186205124-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45763386-C-G

http://identifiers.org/hco/4/GRCh38#186205160-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45763359-A-C

186205160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45763359-A-G

186205164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45763355-C-T

186205178-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45763342-C-G

186205178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45763342-C-T

186205251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45763269-T-C

186205278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45763242-G-A

186205278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45763242-G-T

186205293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45763227-G-A

186205293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45763227-G-T

186205305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45763215-A-G

186205316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45763204-C-T

186205379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45763133-G-A

http://identifiers.org/hco/4/GRCh38#186205382-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45763130-A-C

http://identifiers.org/hco/4/GRCh38#186205397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45763115-C-A

186205405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45763107-G-A

186205417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45763095-G-A

186205417-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45763095-G-T

http://identifiers.org/hco/4/GRCh38#186205421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45763090-C-A

186205439-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45763072-T-A

186205439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45763072-T-C

186205442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45763069-T-C

186205460-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45763050-T-G

186207998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45762176-G-A

186209074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45761612-A-G

186209134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45761553-C-T

186209185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 45761502-C-T

186209258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45761429-C-T

http://identifiers.org/hco/4/GRCh38#186209365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45761327-C-A

186209591-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45761040-A-T

186210103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45760495-A-G

http://identifiers.org/hco/4/GRCh38#186210178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45760382-C-A

186210178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45760382-C-T

186210249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45760317-G-A

186210328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45760259-A-G

186210328-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45760259-A-T

186210367-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45760228-T-G

http://identifiers.org/hco/4/GRCh38#186210416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45760181-C-A

186210630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45759982-G-A

186210633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45759979-G-A

186210682-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45759935-T-G

186210707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45759909-C-T

186210735-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45759882-T-A

186210735-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45759882-T-G

186210818-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45759786-T-A

186211718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45759586-G-A

186211718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45759586-G-T

186211741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45759559-C-T

186211742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45759558-A-G

http://identifiers.org/hco/4/GRCh38#186211857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45759455-C-A

186211876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45759430-G-T

186211908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45759399-C-T

186211950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45759360-G-A

186211950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45759360-G-T

186212254-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45759089-T-G

186212393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45758950-C-T

186212425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23198
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45758918-G-A