http://identifiers.org/hco/1/GRCh38#222618132-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183150847-C-A

222618132-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 183150847-C-G

222618132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 183150847-C-T

http://identifiers.org/hco/1/GRCh38#222618193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183150786-C-A

222618193-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 183150786-C-G

222618207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 183150772-T-C

222618250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 183150729-G-A

222618250-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 183150729-G-C

222618250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 183150729-G-T

http://identifiers.org/hco/1/GRCh38#222618284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183150708-C-A

222618284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183150708-C-T

222618534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183150518-G-A

222618550-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 183150507-T-G

http://identifiers.org/hco/1/GRCh38#222618598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183150461-C-A

222618598-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183150461-C-G

222618686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183150371-G-A

222618702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183150355-G-A

222618706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183150351-A-G

222619150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183149919-A-G

222619214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183149852-C-T

222619578-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183149482-T-G

222619696-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183149370-T-G

222619725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183149343-T-C

http://identifiers.org/hco/1/GRCh38#222619962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183149097-C-A

222620585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183147890-A-G

222620725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183147745-C-T

222620809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183147663-A-G

222620921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183147547-A-G

222621088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183147379-A-G

222621340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183146939-C-T

222621516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183146771-C-T

222622319-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183145682-T-A

222622419-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183145591-C-G

http://identifiers.org/hco/1/GRCh38#222622428-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183145582-A-C

222622428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183145582-A-G

222622591-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183145419-G-C

222622702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183145326-C-T

222622954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183144973-G-T

222623093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183144832-G-T

222623164-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183144766-C-G

222623298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183144665-A-G

222623298-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183144665-A-T

222623309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 183144648-A-G

222623323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 183144607-G-A

222623323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 183144607-G-T

222623453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183144474-C-T

222623494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183144434-A-G

http://identifiers.org/hco/1/GRCh38#222623529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183144403-C-A

222623673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183144261-G-A

222623951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183143994-C-T

222624736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183143505-T-C

222624749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183143492-T-C

222624825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 183143416-A-G

222624825-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 183143416-A-T

http://identifiers.org/hco/1/GRCh38#222624840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183143401-C-A

222624840-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 183143401-C-G

http://identifiers.org/hco/1/GRCh38#222624880-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183143376-C-A

222624880-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183143376-C-G

222624903-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183143353-G-C

222624903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183143353-G-T

222624909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183143347-A-G

http://identifiers.org/hco/1/GRCh38#222625498-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183142678-A-C

222625623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183142565-G-A

222627073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183140768-T-C

222627434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183140482-A-G

222627434-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183140482-A-T

http://identifiers.org/hco/1/GRCh38#222627435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183140481-C-A

222627435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183140481-C-T

http://identifiers.org/hco/1/GRCh38#222627477-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183140445-A-C

222627477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183140445-A-G

222627531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183140403-G-A

222627531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183140403-G-T

222627554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183140380-A-G

222627630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 183140302-T-C

222627718-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 183140217-A-T

222627755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 183140168-C-T

http://identifiers.org/hco/1/GRCh38#222627784-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183140139-A-C

222627811-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 183140112-T-A

222627811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 183140112-T-C

222627811-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 183140112-T-G

222627855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 183140068-A-G

222627855-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 183140068-A-T

222627859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 183140064-A-G

222627896-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 183140027-T-A

222627980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 183139946-G-A

222628016-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 183139910-C-G

222628088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 183139838-G-A

222628248-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 183139675-C-G

222628292-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 183139631-T-G

http://identifiers.org/hco/1/GRCh38#222628293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/1/GRCm39#183139630-C-A

222628379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 183139586-A-G

222628410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 183139555-C-T

222628482-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 183139498-C-G

222628482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 183139498-C-T

http://identifiers.org/hco/1/GRCh38#222628527-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183139453-A-C

222628566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 183139417-T-C

222628628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 183139349-G-A

222628668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 183139309-C-T

222628696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 183139281-C-T

222628701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 183139276-C-T

http://identifiers.org/hco/1/GRCh38#222628733-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183139247-A-C

222628809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 183139168-G-A

222628907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 183139073-G-A

222628907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 183139073-G-T

222629019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 183138961-T-C

222629060-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 183138938-C-G

222629060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 183138938-C-T

222629084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 183138917-T-C

222629156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 183138845-G-A

222629156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 183138845-G-T

222629204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 183138797-G-A

222629214-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 183138787-C-G

222629214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 183138787-C-T

222629227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 183138774-G-A

222629256-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 183138745-A-T

222629285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 183138716-G-A

222629297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 183138710-C-T

222629355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 183138632-G-A

222629384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 183138614-G-A

222629453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 183138545-A-G

222629468-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 183138530-C-G

http://identifiers.org/hco/1/GRCh38#222629551-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183138453-A-C

222629551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 183138453-A-G

222629579-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 183138425-G-C

222629606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 183138398-G-A

222629606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 183138398-G-T

222629673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 183138322-A-G

222629714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 183138281-G-A

222629714-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 183138281-G-C

222629714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 183138281-G-T

222629717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 183138278-A-G

222629717-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 183138278-A-T

222629748-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 183138247-A-T

222630206-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 183137783-A-T

222631564-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183136059-T-A

222631580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183136046-T-C

http://identifiers.org/hco/1/GRCh38#222631767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183135860-C-A

222631841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183135769-C-T

222632041-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183135587-T-G

222632101-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183135536-T-A

222632101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183135536-T-C

222632228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 183135418-T-C

222632392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183135112-T-C

222632437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183135072-A-G

222632441-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183135068-T-A

222632468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183135032-G-A

222632468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183135032-G-T

222632686-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183134813-G-C

222632806-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183134714-T-A

222632806-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183134714-T-G

222632865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183134656-C-T

222632996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183134530-T-C

222633019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183132641-A-G

222633206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 183132448-C-T

222633265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183132383-T-C

222633318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183132167-T-C

222633360-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183132126-A-T

222633397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183132089-T-C

222633397-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183132089-T-G

222633605-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183131927-G-C

http://identifiers.org/hco/1/GRCh38#222633663-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183131884-A-C

222633734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183131836-G-T

222633737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183131833-G-A

222635054-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183130612-G-C

222635309-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183130378-C-G

222635309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183130378-C-T

222635365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183130321-G-A

222635365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183130321-G-T

222635421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183130266-C-T

http://identifiers.org/hco/1/GRCh38#222644181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#183127043-C-A

222644181-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 183127043-C-G

222644181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 183127043-C-T

222644187-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183127037-T-A

222644187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183127037-T-C

222644193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 183127033-T-C

222644203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 183127023-T-C

http://identifiers.org/hco/1/GRCh38#222644218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183127011-C-A

222644218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183127011-C-T

222644226-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 183127003-G-C

222644226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 183127003-G-T

222644237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 183126992-C-T

222644282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183126926-G-A

222644282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183126926-G-T

222644312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 183126896-T-C

http://identifiers.org/hco/1/GRCh38#222644343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#183126865-C-A

222644343-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 183126865-C-G

222644343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 183126865-C-T

222644372-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 183126836-C-G

222644431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 183126782-G-A

222644534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 183126679-T-C

222644571-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 183126642-A-T

222644695-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183126551-T-A

222644706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183126543-G-A

http://identifiers.org/hco/1/GRCh38#222644716-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183126533-C-A

222645031-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183126267-C-G

222645036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183126262-G-A

222645164-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183126152-A-T

222645437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183125899-G-A

222645437-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183125899-G-C

222645437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183125899-G-T

222645742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 183125610-A-G

http://identifiers.org/hco/1/GRCh38#222645761-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183125585-C-A

http://identifiers.org/hco/1/GRCh38#222645847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183125446-C-A

222645847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 183125446-C-T

http://identifiers.org/hco/1/GRCh38#222645851-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183125442-A-C

222645851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 183125442-A-G

222645851-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 183125442-A-T

222645864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 183125429-A-G

222645976-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 183125371-T-G

http://identifiers.org/hco/1/GRCh38#222647167-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183123654-A-C

222648460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183121371-A-G

222648476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183121359-G-A

http://identifiers.org/hco/1/GRCh38#222648589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183121240-C-A

222648696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183120967-G-T

222648744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183120910-A-G

222648885-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183120777-T-A

222648885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183120777-T-C

http://identifiers.org/hco/1/GRCh38#222648905-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183120757-A-C

http://identifiers.org/hco/1/GRCh38#222648982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183120677-C-A

http://identifiers.org/hco/1/GRCh38#222648983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183120676-C-A

222648983-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183120676-C-G

222648983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183120676-C-T

222649201-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183120434-C-G

http://identifiers.org/hco/1/GRCh38#222650187-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183120208-A-C

222650187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183120208-A-G

222650187-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183120208-A-T

http://identifiers.org/hco/1/GRCh38#222650216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183120179-C-A

222650216-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183120179-C-G

222650228-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183120168-T-A

222650228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183120168-T-C

222650562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183119871-A-G

222650723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183119696-T-C

222650761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183119655-G-A

222650761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183119655-G-T

http://identifiers.org/hco/1/GRCh38#222650769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183119643-C-A

222650769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183119643-C-T

222650789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 183119620-G-A

222650789-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 183119620-G-T

222650877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 183119530-G-A

222650877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 183119530-G-T

222650908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183119499-G-T

http://identifiers.org/hco/1/GRCh38#222650916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183119491-C-A

222650982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183119438-C-T

http://identifiers.org/hco/1/GRCh38#222650987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183119433-C-A

222651052-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183119371-T-A

222651122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183119301-G-A

222651958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183117989-T-C

222652019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 183117928-A-G

222652061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183117886-G-A

222652061-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183117886-G-C

222652061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183117886-G-T

222652324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, missense_variant
orthologous variants: 183117380-A-G

222652462-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron variant
orthologous variants: 183117290-T-A

222652462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron variant
orthologous variants: 183117290-T-C

222652584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron variant
orthologous variants: 183117183-A-G

222652857-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron variant
orthologous variants: 183116940-C-G

222652861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron variant
orthologous variants: 183116936-G-A

222652861-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron variant
orthologous variants: 183116936-G-C

222652861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron variant
orthologous variants: 183116936-G-T

222652915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron variant
orthologous variants: 183116689-A-G

222652962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron variant
orthologous variants: 183116648-G-A

222652962-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron variant
orthologous variants: 183116648-G-C

222654040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron variant
orthologous variants: 183115685-A-G

222654133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron variant
orthologous variants: 183115587-T-C

222654133-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron variant
orthologous variants: 183115587-T-G

222654185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron variant
orthologous variants: 183115540-T-C

222654208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron variant
orthologous variants: 183115520-G-A

222654246-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: missense variant
orthologous variants: 183115487-A-T

222654250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: synonymous variant
orthologous variants: 183115483-G-T

222654316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron variant
orthologous variants: 183115417-G-T

222654327-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron variant
orthologous variants: 183115406-G-C

222654339-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron variant
orthologous variants: 183115394-T-G

222654357-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron variant
orthologous variants: 183115378-T-A

222654357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron variant
orthologous variants: 183115378-T-C

http://identifiers.org/hco/1/GRCh38#222654524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183115212-C-A

222654524-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron variant
orthologous variants: 183115212-C-G

222654524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron variant
orthologous variants: 183115212-C-T

222654654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: splice acceptor variant
orthologous variants: 183115101-G-T

222654686-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: missense variant
orthologous variants: 183115069-C-G

222654686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: synonymous variant
orthologous variants: 183115069-C-T

222658673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 183113828-G-T

http://identifiers.org/hco/1/GRCh38#222658674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183113827-C-A

222658674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 183113827-C-T

http://identifiers.org/hco/1/GRCh38#222658675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183113826-C-A

222658675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 183113826-C-T

222658800-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 183113701-T-A

http://identifiers.org/hco/1/GRCh38#222658834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183113667-C-A

222658834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183113667-C-T

http://identifiers.org/hco/1/GRCh38#222658940-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183113515-A-C

222659243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 183112992-T-C

222659320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 183112919-A-G

222659460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 183112539-A-G

222659461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 183112538-T-C

222659547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 183112455-G-A

222659558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 183112434-A-G

222659568-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 183112424-G-C

222659669-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 183112300-T-A

http://identifiers.org/hco/1/GRCh38#222659679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183112290-C-A

222659679-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 183112290-C-G

222659679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 183112290-C-T

http://identifiers.org/hco/1/GRCh38#222659949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183112002-C-A

http://identifiers.org/hco/1/GRCh38#222660327-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183111637-A-C

222660327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 183111637-A-G

222660444-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 183111550-T-A

222660444-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 183111550-T-G

http://identifiers.org/hco/1/GRCh38#222662163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183110743-C-A

222662196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183110725-T-C

222662196-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183110725-T-G

222662313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 183110618-G-A

222662614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183110319-T-C

222662815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183110167-G-A

222662873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183110112-G-T

222663056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183109998-T-C

http://identifiers.org/hco/1/GRCh38#222663135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183109971-C-A

222663168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183109945-T-C

222663168-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183109945-T-G

222663226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183109886-A-G

http://identifiers.org/hco/1/GRCh38#222663234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183109878-C-A

222663234-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183109878-C-G

222663637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183109509-A-G

222663860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183109296-G-A

222663860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183109296-G-T

222663861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183109295-T-C

http://identifiers.org/hco/1/GRCh38#222664258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183108952-C-A

222664375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183108845-T-C

222664457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183108776-T-C

222664469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183108763-C-T

222664535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183108693-G-A

222665259-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183108553-A-T

222665354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 183108461-G-A

222665354-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 183108461-G-C

222665356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 183108459-G-A

222665491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 183108324-G-A

222665506-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 183108306-C-G

222665506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 183108306-C-T

222665558-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: missense variant
orthologous variants: 183108254-C-G

222665560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: missense variant
orthologous variants: 183108252-C-T

222665674-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: 3 prime UTR variant
orthologous variants: 183108140-A-T

http://identifiers.org/hco/1/GRCh38#222665908-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183107897-A-C

http://identifiers.org/hco/1/GRCh38#222666247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183107571-C-A

222666484-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: 3 prime UTR variant
orthologous variants: 183106839-T-A

222666487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: 3 prime UTR variant
orthologous variants: 183106836-G-A

222666487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: 3 prime UTR variant
orthologous variants: 183106836-G-T

http://identifiers.org/hco/1/GRCh38#222666537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183106796-C-A

222666537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: 3 prime UTR variant
orthologous variants: 183106796-C-T

222666542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: 3 prime UTR variant
orthologous variants: 183106791-A-G

222666544-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: 3 prime UTR variant
orthologous variants: 183106789-C-G

222666583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: 3 prime UTR variant
orthologous variants: 183106753-T-C

222666621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: 3 prime UTR variant
orthologous variants: 183106721-A-G

http://identifiers.org/hco/1/GRCh38#222666994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183106581-C-A

http://identifiers.org/hco/1/GRCh38#222667080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183106499-C-A

http://identifiers.org/hco/1/GRCh38#222667120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183106458-C-A

222667266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: 3 prime UTR variant
orthologous variants: 183106371-G-T

222667305-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: 3 prime UTR variant
orthologous variants: 183106092-T-A

222667305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: 3 prime UTR variant
orthologous variants: 183106092-T-C

222667486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: 3 prime UTR variant
orthologous variants: 183105824-A-G

222667653-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: 3 prime UTR variant
orthologous variants: 183105669-G-C

222667653-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: 3 prime UTR variant
orthologous variants: 183105669-G-T

222667726-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: 3 prime UTR variant
orthologous variants: 183105608-A-T

222667736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24008
most severe consequence: 3 prime UTR variant
orthologous variants: 183105596-T-C