http://identifiers.org/hco/1/GRCh38#162630939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169939840-C-A

162631033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 169939745-C-T

162631343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant
orthologous variants: 169939498-T-C

162631343-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant
orthologous variants: 169939498-T-G

162631483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169939366-T-C

http://identifiers.org/hco/1/GRCh38#162631508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#169939349-C-A

162631527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169939339-T-C

162631582-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169939292-T-A

162631582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169939292-T-C

162631616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169939258-G-A

162631616-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169939258-G-C

162631616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169939258-G-T

http://identifiers.org/hco/1/GRCh38#162631738-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169939131-A-C

http://identifiers.org/hco/1/GRCh38#162631907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169938964-C-A

162631907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169938964-C-T

162631921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169938868-G-A

162631921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169938868-G-T

162631938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169938857-G-T

162631989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 169938806-A-G

162632143-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, undefined
orthologous variants: 169938667-G-C

162632143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, undefined
orthologous variants: 169938667-G-T

162632157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169938653-C-T

162632181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, undefined
orthologous variants: 169938629-A-G

162632181-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, undefined
orthologous variants: 169938629-A-T

162632191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, undefined
orthologous variants: 169938622-G-T

162632209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169938604-A-G

http://identifiers.org/hco/1/GRCh38#162632543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#169938272-C-A

162632543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 169938272-C-T

162632751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169938062-G-A

162632751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169938062-G-T

162633436-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169937405-A-T

http://identifiers.org/hco/1/GRCh38#162633828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169937048-C-A

162633908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169936998-A-G

162634079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169936830-G-A

162634373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169936576-G-A

162634628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169936085-C-T

162635000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169935776-G-T

162635001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169935775-G-A

162635116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169935679-C-T

162635292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169935543-C-T

162635611-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169935267-C-G

162635611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169935267-C-T

162635662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169935226-C-T

162635734-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169935113-C-G

162635862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169934991-T-C

http://identifiers.org/hco/1/GRCh38#162636031-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169934862-A-C

162636040-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169934853-T-A

162636040-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169934853-T-G

162636076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169934819-A-G

162636639-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169934229-C-G

162637261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169932768-T-C

162637279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169932749-G-A

http://identifiers.org/hco/1/GRCh38#162637380-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169932645-A-C

162637453-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169932549-C-G

162637775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169932269-A-G

162637849-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169932211-G-C

162639714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169930546-G-A

162640435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169929910-G-A

162640599-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169929756-T-A

162640671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169929683-T-C

http://identifiers.org/hco/1/GRCh38#162641273-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169929016-A-C

162645541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

162645553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-T

162645594-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-C

162645976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169923572-T-C

162645988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169923560-T-C

162646127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169923440-G-A

162646657-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169922161-G-C

162646904-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169921929-T-A

162646904-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169921929-T-G

162647108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169921695-T-C

162647176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169921633-A-G

162647301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169921501-G-A

162648104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169921308-A-G

162648149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169921263-C-T

162648225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169921209-G-A

162648322-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169921118-A-T

162648432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169921022-A-G

162648432-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169921022-A-T

http://identifiers.org/hco/1/GRCh38#162648541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169920877-C-A

162648806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169920684-G-A

162648911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169920609-G-A

http://identifiers.org/hco/1/GRCh38#162648993-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169920537-A-C

162649117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169920417-T-C

162649150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169920370-G-A

162649176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169920344-G-A

162649317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169919835-C-T

162649542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169919583-A-G

162649542-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169919583-A-T

162649553-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169919565-T-G

162649574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169919544-A-G

162649582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169919536-A-G

162649756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169919379-G-A

162650040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169919084-T-C

162650139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169918981-G-A

http://identifiers.org/hco/1/GRCh38#162650659-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169918791-A-C

162650683-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169918767-C-G

162651202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169918544-T-C

162651213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169918533-T-C

http://identifiers.org/hco/1/GRCh38#162651229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169918525-C-A

162651258-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169918500-C-G

162651267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169918491-C-T

162651350-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169918411-T-A

162651364-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169918398-T-A

162651378-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169918386-A-T

162653195-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169917848-G-C

162653196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169917847-T-C

162654648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169917050-A-G

162654681-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169917017-T-A

162654681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169917017-T-C

162654739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169916949-A-G

162654739-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169916949-A-T

http://identifiers.org/hco/1/GRCh38#162654748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169916937-C-A

162654748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169916937-C-T

http://identifiers.org/hco/1/GRCh38#162654769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169916916-C-A

162655029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169916683-C-T

162655032-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169916681-G-T

162655096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169916619-G-A

162655096-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169916619-G-T

162655161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169916568-G-T

162655163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169916566-G-A

162655214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 169916519-C-T

162655234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 169916499-G-T

162655267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 169916466-A-G

162655315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 169916421-A-G

162655316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 169916420-G-T

162655336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 169916400-A-G

http://identifiers.org/hco/1/GRCh38#162655347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169916389-C-A

162655363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 169916373-G-A

162655363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 169916373-G-T

http://identifiers.org/hco/1/GRCh38#162655367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169916369-C-A

162655367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 169916369-C-T

162655804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169916191-A-G

162655853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169916142-C-T

162656323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169915562-G-A

162656470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169915425-C-T

162656679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169915229-A-G

162656780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169915129-C-T

162657262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169914948-C-T

http://identifiers.org/hco/1/GRCh38#162659189-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169913540-A-C

162659199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169913530-A-G

162659205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169913524-G-A

162659478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169913026-C-T

162659961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169912559-A-G

162661380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169912140-T-C

162661429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169912091-T-C

162661573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169911936-G-A

162661790-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169911718-G-C

162661916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169911612-C-T

162661952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169911577-G-A

http://identifiers.org/hco/1/GRCh38#162662044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169911478-C-A

162662044-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169911478-C-G

162663417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 169911314-G-A

162663601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169911198-G-A

162663601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169911198-G-T

162663747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169911097-G-A

162663751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169911093-T-C

162664052-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169910815-G-C

162664057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169910810-G-A

162664057-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169910810-G-C

162664139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169910743-T-C

162664277-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169910630-T-G

162664348-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169910562-A-T

162664830-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169909676-C-G

162664830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169909676-C-T

162664849-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169909658-T-A

162664939-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169909562-C-G

162664981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169909480-T-C

http://identifiers.org/hco/1/GRCh38#162665212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169909279-C-A

162665387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169909102-T-C

162665483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169909024-T-C

162665483-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169909024-T-G

162665579-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169908941-T-G

162666339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169908722-G-A

162666420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169908645-C-T

http://identifiers.org/hco/1/GRCh38#162666435-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169908630-A-C

162666461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169908606-G-A

http://identifiers.org/hco/1/GRCh38#162666566-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169908532-A-C

http://identifiers.org/hco/1/GRCh38#162666567-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169908524-A-C

162666607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169908484-A-G

162666876-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169908080-C-G

162666895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169908056-T-C

162667132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169907827-A-G

162667137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169907822-T-C

162667419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169907540-A-G

162667524-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169907432-C-G

162667610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169907369-C-T

162667842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169907176-T-C

http://identifiers.org/hco/1/GRCh38#162668036-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169907035-A-C

http://identifiers.org/hco/1/GRCh38#162668077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169907017-C-A

162668217-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169906865-A-T

162668260-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169906842-C-G

162668289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169906812-G-A

162668362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169906740-G-T

162668570-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169906537-T-A

162668650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169906467-G-T

162668734-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169906407-C-G

162668734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169906407-C-T

162668750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169906391-A-G

162668880-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169906325-A-T

162669096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169906155-A-G

162669294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169905958-G-A

162669294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169905958-G-T

162670686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169903380-C-T

162670687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169903379-G-A

162671218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169902818-A-G

162671434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169902414-A-G

162671563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169902308-T-C

162671619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 169902256-C-T

162671982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169901914-A-G

http://identifiers.org/hco/1/GRCh38#162672016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169901877-C-A

162672349-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169901534-C-G

162672780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169899929-G-A

162673225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169899491-G-T

162673295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169899436-T-C

162673409-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 169899323-A-T

162673429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169899303-A-G

162674804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169898491-C-T

162675185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169898423-G-T

162675239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169898370-G-A

162675251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169898358-G-A

162675376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169898249-T-C

162675376-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169898249-T-G

162675662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169897532-G-A

162676011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169897209-G-A

162676061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169897160-G-A

162676756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169896556-A-G

162677021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169896309-G-A

162677021-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169896309-G-C

162677043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169896286-G-A

162677258-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 169896089-C-G

162677461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169895857-T-C

162677857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169894858-C-T

162678084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169893885-C-T

162678437-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 169893638-T-A

162678437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 169893638-T-C

162678507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 169893568-G-A

162678742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 169893340-G-A

162680781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169892967-G-A

162681199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169892573-C-T

http://identifiers.org/hco/1/GRCh38#162681316-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169892487-A-C

162681636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169892170-G-A

http://identifiers.org/hco/1/GRCh38#162681737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169892101-C-A

162681927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169891921-G-A

162682152-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169891693-G-C

162682276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169891571-C-T

162682290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169891557-G-A

162682457-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169891407-G-C

162682647-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169891255-G-C

162683144-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169890832-T-G

162683180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169890791-G-A

162683242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169890726-T-C

162684339-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169890453-C-G

162684360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169890432-T-C

http://identifiers.org/hco/1/GRCh38#162684468-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169889827-A-C

http://identifiers.org/hco/1/GRCh38#162684474-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169889821-C-A

162684474-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169889821-C-G

162684678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169889637-G-A

162685006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169889299-G-A

162685220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169889109-T-C

162685623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169888758-G-A

162685697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169888693-C-T

http://identifiers.org/hco/1/GRCh38#162685778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169888611-C-A

162685811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169888580-A-G

162686049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169888379-A-G

162686049-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169888379-A-T

162687099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169888140-T-C

162687154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169888076-G-A

162687178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169888052-A-G

162687208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169888027-G-T

162687215-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169888020-T-G

162687737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169887361-G-A

162688341-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169886184-T-G

162688440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169886086-A-G

162688852-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169885698-T-G

162689106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169885464-C-T

162689113-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169885457-C-G

http://identifiers.org/hco/1/GRCh38#162689195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169885371-C-A

162689195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169885371-C-T

162689258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169885305-G-A

162689258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169885305-G-T

162689441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169885131-C-T

162689458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169885114-A-G

162689552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169885031-G-T

http://identifiers.org/hco/1/GRCh38#162689712-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169884871-A-C

162690249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 169884766-A-G

162690746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169884297-G-A

162691092-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 169883961-C-G

162691174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 169883878-G-A

162691354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169883719-A-G

162691955-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169882575-A-T

162691976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169882542-G-A

162692232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169882294-T-C

162692353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169882196-A-G

162692476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169882084-A-G

162692709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169882022-T-C

162692889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169881891-C-T

162692911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169881870-T-C

http://identifiers.org/hco/1/GRCh38#162693011-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169881770-A-C

162695576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169881294-G-A

162695723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169881176-G-A

162696067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169880829-A-G

162696090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169880807-A-G

162696979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169879980-C-T

162697002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169879957-C-T

162697189-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169879821-A-T

162697260-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169879747-G-T

162698045-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169878986-T-A

http://identifiers.org/hco/1/GRCh38#162698213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169878823-C-A

162698213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169878823-C-T

162698241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169878795-G-A

162698311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169878742-G-A

162698334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169878714-A-G

162698334-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169878714-A-T

162699425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169878593-G-A

http://identifiers.org/hco/1/GRCh38#162699614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#169878446-C-A

162699693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169878412-C-T

http://identifiers.org/hco/1/GRCh38#162699877-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169877948-A-C

162700250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169877573-A-G

162700628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169877344-G-T

162700913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169877055-G-T

http://identifiers.org/hco/1/GRCh38#162705003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169876309-C-A

162705003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169876309-C-T

http://identifiers.org/hco/1/GRCh38#162705036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169876278-C-A

162705036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169876278-C-T

162705145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169876168-G-T

162705227-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169876091-C-G

162705324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169875997-C-T

http://identifiers.org/hco/1/GRCh38#162705532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169875790-C-A

162709295-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169872067-G-C

162709409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169871954-G-A

162709520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169871891-T-C

162709823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169871547-G-T

162709967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169871406-T-C

162709973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169871400-C-T

162710043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169871330-G-A

162710047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169871326-T-C

162710120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169871253-T-C

162710594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169870795-A-G

162710733-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169870676-A-T

162710827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169870607-T-C

http://identifiers.org/hco/1/GRCh38#162711042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169870451-C-A

162711042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169870451-C-T

162711075-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169870418-A-T

162711241-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169870271-T-G

162711309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169870220-A-G

162711516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169869996-T-C

162711547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169869964-A-G

162711741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169869791-C-T

162711744-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169869788-C-G

162711744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169869788-C-T

162711749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169869783-C-T

162711860-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169869258-A-T

162711871-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169869247-T-G

162712169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169868964-A-G

162712170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169868963-T-C

162712177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169868956-A-G

162712392-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169868817-C-G

162712392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169868817-C-T

162712529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169868683-G-A

162712529-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169868683-G-C

162712658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169868558-C-T

162712662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169868554-C-T

162712881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169868339-G-A

162713254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169867962-C-T

162713657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169867263-T-C

162714467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169866319-G-T

http://identifiers.org/hco/1/GRCh38#162714605-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169866181-A-C

162714605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169866181-A-G

162714639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169866148-A-G

162714849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169865659-A-G

162714915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169865586-T-C

162714948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169865553-G-A

162714983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169865521-C-T

162714984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169865520-A-G

162714997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169865507-T-C

162715374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169865180-G-A

162715374-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169865180-G-C

162718000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169864769-A-G

162718058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169864711-A-G

162718093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169864676-T-C

162718159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169864581-C-T

162718203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169864505-A-G

162718291-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169864409-A-T

162718392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169864289-C-T

162718720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169863873-T-C

162718896-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169863725-T-A

162718960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169863661-A-G

162718999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169863622-T-C

162719020-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169863605-T-A

162719256-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169863371-T-G

162719273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169863360-T-C

162719273-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169863360-T-G

162719284-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169863349-T-A

162719284-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169863349-T-G

162719459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169863185-C-T

162719647-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169862995-T-A

162719647-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169862995-T-G

162719837-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169862805-C-G

162720344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169861462-T-C

162720349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169861457-C-T

162720410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169861398-A-G

162720486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169861326-G-A

162720521-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169861292-T-A

162720618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169861210-T-C

162720946-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169860858-A-T

162721132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169860679-A-G

162721149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169860662-G-A

162721326-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169860505-T-G

http://identifiers.org/hco/1/GRCh38#162721525-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169860308-A-C

162721560-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169860274-T-G

162722263-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169859175-T-A

162722323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169859121-C-T

162722376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169859072-A-G

http://identifiers.org/hco/1/GRCh38#162722641-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169858807-A-C

162722651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169858797-A-G

162724427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169858641-A-G

162724641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169858452-G-A

162724846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169858276-G-A

162724992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169858150-T-C

162725057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169858086-G-A

162725120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169858004-T-C

162725176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169857968-A-G

162725252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169857893-A-G

162726213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169856890-G-A

162726213-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169856890-G-C

162726543-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169855618-C-G

162728410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169855111-G-T

162728487-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169855028-G-C

162728560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169854956-A-G

162729080-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169854074-T-A

http://identifiers.org/hco/1/GRCh38#162729108-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169854046-A-C

162729448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169853785-A-G

162730072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169853486-A-G

162730073-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169853485-A-T

162730091-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169853467-G-T

162730273-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169853289-C-G

162730484-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169853104-A-T

162730639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169842611-G-T

162731103-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169842215-T-G

162731286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169841428-A-G

162731286-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169841428-A-T

162731379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169841269-T-C

162731604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169841044-A-G

162731701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169840958-A-G

162731735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169840924-G-T

http://identifiers.org/hco/1/GRCh38#162732113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169839632-C-A

http://identifiers.org/hco/1/GRCh38#162732212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#169839569-C-A

162732212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 169839569-C-T

162732223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169839556-C-T

162732243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169839536-A-G

162732343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169839495-G-A

162732348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169839490-C-T

162732502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169839355-G-A

162732680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169839177-G-A

162732761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169839105-G-A

162733077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169838791-G-A

162733105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169838772-G-A

162733219-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169838657-A-T

162733361-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169838525-G-C

162733375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169838511-G-A

162733548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169838335-A-G

http://identifiers.org/hco/1/GRCh38#162735627-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169836553-A-C

162735645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169836535-C-T

http://identifiers.org/hco/1/GRCh38#162735648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169836532-C-A

162735717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169836406-A-G

162735925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169836229-A-G

162735948-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169836206-C-G

162735948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169836206-C-T

162735963-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169836191-G-C

162735978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169836176-A-G

162735978-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169836176-A-T

162736047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169836124-C-T

162736142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169836033-T-C

162752307-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169835124-A-T

162752360-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169835080-C-G

162752626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169834888-A-G

162752864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169834649-A-G

162752943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169834580-G-A

162752953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169834570-T-C

http://identifiers.org/hco/1/GRCh38#162752964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169834559-C-A

162753048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169834476-A-G

162753048-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169834476-A-T

162753059-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169834465-T-A

162753059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169834465-T-C

162753059-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169834465-T-G

http://identifiers.org/hco/1/GRCh38#162753083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169834441-C-A

162753083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169834441-C-T

162753084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169834440-T-C

162753251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169834265-G-T

162753255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169834261-A-G

162753264-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169834252-T-A

162753264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169834252-T-C

162753273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169834243-G-A

162753273-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169834243-G-C

162753273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169834243-G-T

162753306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169834210-G-A

162753306-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169834210-G-C

http://identifiers.org/hco/1/GRCh38#162753337-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169834181-C-A

162753337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169834181-C-T

162753603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169833923-C-T

162753643-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169833891-G-C

162753672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169833863-C-T

162753802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169833730-A-G

162754111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169833416-C-T

162754148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169833380-T-C

162754178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169833351-A-G

162754296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169833209-G-A

162754463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169833038-G-A

162754488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169833012-G-A

http://identifiers.org/hco/1/GRCh38#162754556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169832936-C-A

162754556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169832936-C-T

http://identifiers.org/hco/1/GRCh38#162754676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169832819-C-A

162754676-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 169832819-C-G

162754676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 169832819-C-T

162754814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 169832681-G-A

162754896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169832622-A-G

162755389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169832136-G-A

162755520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169832001-G-A

162755521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169832000-G-A

http://identifiers.org/hco/1/GRCh38#162755522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169831999-C-A

162755522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169831999-C-T

162755583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169831937-T-C

162755583-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169831937-T-G

162755894-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169831616-T-A

162756074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169831420-G-A

162756074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169831420-G-T

http://identifiers.org/hco/1/GRCh38#162756583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169830992-C-A

162756583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169830992-C-T

http://identifiers.org/hco/1/GRCh38#162759679-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169829695-A-C

162759713-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169829660-A-T

162759845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 169829530-G-A

162759912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 169829463-G-A

162760030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169829357-G-A

162760030-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169829357-G-C

162760061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169829331-G-A

http://identifiers.org/hco/1/GRCh38#162760130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169829254-C-A

162761174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169825778-G-A

162761179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169825773-A-G

162761179-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169825773-A-T

162761262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 169825690-C-T

162761277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 169825675-T-C

http://identifiers.org/hco/1/GRCh38#162761394-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169825558-A-C

162761394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 169825558-A-G

162761457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169825495-A-G

http://identifiers.org/hco/1/GRCh38#162761470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169825480-C-A

162761470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169825480-C-T

162761602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169825349-G-A

162761602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169825349-G-T

http://identifiers.org/hco/1/GRCh38#162761604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169825347-C-A

162761604-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169825347-C-G

162761758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169825200-A-G

162761789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169825169-A-G

162761834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169825122-A-G

162764371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169824825-G-A

162764371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169824825-G-T

162764380-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169824816-T-A

162764418-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169824795-T-A

162764418-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169824795-T-G

162764493-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169824719-G-C

162765097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169824332-A-G

http://identifiers.org/hco/1/GRCh38#162765232-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169824021-A-C

162765232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169824021-A-G

162765238-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169824015-A-T

162765273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169823984-C-T

162765412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169823859-A-G

162765436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169823839-G-A

162765866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169823393-G-A

162765866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169823393-G-T

http://identifiers.org/hco/1/GRCh38#162765898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169823285-C-A

162765898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169823285-C-T

162766169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169823012-G-A

162766169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169823012-G-T

162766181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169823000-T-C

162766181-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169823000-T-G

162766182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169822999-G-A

162766182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169822999-G-T

http://identifiers.org/hco/1/GRCh38#162767126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169822384-C-A

162767126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169822384-C-T

162767155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169822355-T-C

162767300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 169822211-C-T

162767362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169822149-G-A

162767436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169821683-A-G

162767481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169821636-A-G

http://identifiers.org/hco/1/GRCh38#162767482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169821635-C-A

162767482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169821635-C-T

162767484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169821633-A-G

162767908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169820843-G-A

162767953-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169820806-T-A

162767973-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169820770-T-G

162768069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169820673-G-A

162768119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169820630-C-T

162768239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169820443-G-A

162768439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169820256-C-T

162768578-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169820164-C-G

162768674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169820072-C-T

162768699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169820057-T-C

162768725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169820031-T-C

162768734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169820022-G-T

162768760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169819996-A-G

162768868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169819884-C-T

162768874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169819880-A-G

162768910-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169819844-G-C

162768978-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169819748-T-G

162769154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169819242-G-A

162769364-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169819036-C-G

162769452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169818953-A-G

http://identifiers.org/hco/1/GRCh38#162769614-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169818807-A-C

162769884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169818596-G-A

162770171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169818305-G-A

162770245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169818243-A-G

162770250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169818240-T-C

162770252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169818238-G-T

162770513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 169817999-G-A

162770513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 169817999-G-T

162770544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 169817968-G-A

http://identifiers.org/hco/1/GRCh38#162770589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169817925-C-A

http://identifiers.org/hco/1/GRCh38#162770687-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169817835-A-C

http://identifiers.org/hco/1/GRCh38#162770730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169817792-C-A

162770732-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 169817790-T-A

162770732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 169817790-T-C

162770736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 169817786-A-G

http://identifiers.org/hco/1/GRCh38#162770781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169817747-C-A

http://identifiers.org/hco/1/GRCh38#162770863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169817666-C-A

http://identifiers.org/hco/1/GRCh38#162770874-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169817655-A-C

162771245-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169817094-G-C

162771466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169816769-G-A

162771760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169816444-C-T

162771875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169816327-G-T

162771914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169816289-A-G

162772046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 169816177-A-G

162772442-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169815776-T-A

162772550-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169815668-G-T

162772578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169815641-G-A

162772583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169815636-G-T

162772668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169815535-C-T

162772780-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169815422-T-G

http://identifiers.org/hco/1/GRCh38#162772865-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169815337-A-C

162772883-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169815311-T-G

162772930-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169815263-C-G

162773099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169815096-T-C

162773119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169815076-T-C

162773144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169815045-G-A

162773347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169814832-T-C

162773395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169814785-G-T

162773419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169814761-G-T

162773436-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169814744-T-G

162773446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169814734-G-A

162773684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169814487-T-C

162773692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169814479-G-T

162773815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169814356-G-A

162773891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169814302-A-G

162774267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169813924-G-A

http://identifiers.org/hco/1/GRCh38#162774317-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169813878-A-C

162774416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169813778-C-T

162774602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169813624-A-G

162774670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169813571-C-T

162774995-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169813257-T-A

162775109-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169813174-C-G

162775449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169812838-A-G

162775449-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169812838-A-T

162775574-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169812709-G-C

162775629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169812655-A-G

162775629-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169812655-A-T

162775740-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: missense variant
orthologous variants: 169812544-C-G

162775740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: missense variant
orthologous variants: 169812544-C-T

162775800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: missense variant
orthologous variants: 169812484-C-T

162775881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169812407-A-G

http://identifiers.org/hco/1/GRCh38#162775914-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169812373-A-C

162775924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169812363-A-G

162775943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169812345-G-T

http://identifiers.org/hco/1/GRCh38#162775987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169812297-C-A

http://identifiers.org/hco/1/GRCh38#162776042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169812243-C-A

162776069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169812223-G-T

162776114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169812195-G-A

162776114-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169812195-G-C

162776114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169812195-G-T

http://identifiers.org/hco/1/GRCh38#162776116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169812193-C-A

http://identifiers.org/hco/1/GRCh38#162776541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169811750-C-A

162776541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169811750-C-T

162776605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169811680-T-C

162776606-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169811679-T-G

162776677-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169811611-C-G

http://identifiers.org/hco/1/GRCh38#162777015-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169811309-A-C

162777015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169811309-A-G

162777053-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169811270-G-C

162777221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169811111-T-C

162777571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169810554-C-T

162777671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169810444-A-G

162777962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 169810382-G-A

162778078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169810335-A-G

162778078-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169810335-A-T

162778244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169810188-C-T

162778298-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169810134-C-G

162778298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169810134-C-T

http://identifiers.org/hco/1/GRCh38#162778443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169809935-C-A

162778443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169809935-C-T

http://identifiers.org/hco/1/GRCh38#162778445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169809933-C-A

162778445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169809933-C-T

162778526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169809855-G-A

162778526-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169809855-G-C

162778526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169809855-G-T

162778539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169809842-C-T

162778688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: missense variant
orthologous variants: 169809585-A-G

162779216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169809191-C-T

162779256-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169809151-G-C

162779261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169809146-G-A

162779393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169809020-A-G

162779433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169808981-T-C

162779909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169805730-T-C

http://identifiers.org/hco/1/GRCh38#162779976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169805676-C-A

162779976-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169805676-C-G

162779976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169805676-C-T

http://identifiers.org/hco/1/GRCh38#162779977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169805675-C-A

162780052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169805603-C-T

162780102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169805566-G-A

162780102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: intron variant
orthologous variants: 169805566-G-T

162780311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 3 prime UTR variant
orthologous variants: 169805355-A-G

http://identifiers.org/hco/1/GRCh38#162780604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169805064-C-A

162780667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 3 prime UTR variant
orthologous variants: 169804998-A-G

162780781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 3 prime UTR variant
orthologous variants: 169804808-T-C

162780794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 3 prime UTR variant
orthologous variants: 169804795-C-T

162780967-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 3 prime UTR variant
orthologous variants: 169804638-A-T

162780985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 3 prime UTR variant
orthologous variants: 169804627-G-T

162781118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 3 prime UTR variant
orthologous variants: 169804529-G-T

162781248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 3 prime UTR variant
orthologous variants: 169804411-G-T

162781390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 3 prime UTR variant
orthologous variants: 169804274-T-C

162781390-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 3 prime UTR variant
orthologous variants: 169804274-T-G

http://identifiers.org/hco/1/GRCh38#162781416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169804254-C-A

162781441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 3 prime UTR variant
orthologous variants: 169804232-G-T

http://identifiers.org/hco/1/GRCh38#162781664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169804068-C-A

162781664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 3 prime UTR variant
orthologous variants: 169804068-C-T

162781770-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 3 prime UTR variant
orthologous variants: 169803952-C-G

162781816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 3 prime UTR variant
orthologous variants: 169803906-G-A

162782178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 3 prime UTR variant
orthologous variants: 169803609-G-A

http://identifiers.org/hco/1/GRCh38#162782375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169803426-C-A

162782917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 3 prime UTR variant
orthologous variants: 169803125-G-T

162783187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 3 prime UTR variant
orthologous variants: 169802878-G-T

http://identifiers.org/hco/1/GRCh38#162783377-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169802600-C-A

162783429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 3 prime UTR variant
orthologous variants: 169802532-A-G

162783464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 3 prime UTR variant
orthologous variants: 169802495-A-G

http://identifiers.org/hco/1/GRCh38#162783487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169802473-C-A

162783487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 3 prime UTR variant
orthologous variants: 169802473-C-T

http://identifiers.org/hco/1/GRCh38#162783498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169802462-C-A

162783498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 3 prime UTR variant
orthologous variants: 169802462-C-T

162783499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 3 prime UTR variant
orthologous variants: 169802461-A-G

http://identifiers.org/hco/1/GRCh38#162783558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169802404-C-A

162783703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 3 prime UTR variant
orthologous variants: 169802275-T-C

162783732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 3 prime UTR variant
orthologous variants: 169802248-A-G

162783753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 3 prime UTR variant
orthologous variants: 169802227-G-A

162783809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 3 prime UTR variant
orthologous variants: 169802159-A-G

162783817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 3 prime UTR variant
orthologous variants: 169802151-G-A

162783817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 3 prime UTR variant
orthologous variants: 169802151-G-T

http://identifiers.org/hco/1/GRCh38#162784141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169801892-C-A

162784141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 3 prime UTR variant
orthologous variants: 169801892-C-T

162784164-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 3 prime UTR variant
orthologous variants: 169801869-C-G

162784164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 3 prime UTR variant
orthologous variants: 169801869-C-T

162784250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 3 prime UTR variant
orthologous variants: 169801786-T-C

162784390-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 3 prime UTR variant
orthologous variants: 169801656-G-C

162784605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 3 prime UTR variant
orthologous variants: 169801460-G-T

162784754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 3 prime UTR variant
orthologous variants: 169801356-G-A

162785234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 3 prime UTR variant
orthologous variants: 169800884-A-G

162785293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 3 prime UTR variant
orthologous variants: 169800828-G-A

162785836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 3 prime UTR variant
orthologous variants: 169800384-A-G

162785894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 3 prime UTR variant
orthologous variants: 169800374-C-T

162786359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 3 prime UTR variant
orthologous variants: 169800089-T-C

162786394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 3 prime UTR variant
orthologous variants: 169800054-A-G

162786760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 3 prime UTR variant
orthologous variants: 169799708-T-C

162787123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 3 prime UTR variant
orthologous variants: 169799385-T-C

162787222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 3 prime UTR variant
orthologous variants: 169798472-T-C

162787237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2731
most severe consequence: 3 prime UTR variant
orthologous variants: 169798460-G-A