36740802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29376912-G-T

36740899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29376996-A-G

http://identifiers.org/hco/6/GRCh38#36740909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29377004-C-A

36740909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29377004-C-T

36741067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29377126-A-G

36741150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29377181-G-A

36741150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29377181-G-T

http://identifiers.org/hco/6/GRCh38#36741260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29377283-C-A

http://identifiers.org/hco/6/GRCh38#36741276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29377299-C-A

36741276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29377299-C-T

36741288-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29377311-G-C

36741291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29377314-A-G

36741291-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29377314-A-T

36741390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29377418-T-C

36741411-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29377433-G-C

36741411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29377433-G-T

http://identifiers.org/hco/6/GRCh38#36741436-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29377457-A-C

36741436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29377457-A-G

36741636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29377591-G-A

36741636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29377591-G-T

http://identifiers.org/hco/6/GRCh38#36741651-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29377609-C-A

36741805-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29377674-T-G

http://identifiers.org/hco/6/GRCh38#36741865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29377723-C-A

36741865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29377723-C-T

36741898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29377749-G-T

36741940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29377787-G-T

36741948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29377795-G-A

36741951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29377798-G-A

36741951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29377798-G-T

36741969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29377816-A-G

36742077-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29377860-T-G

36742101-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29377884-G-C

36742101-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29377884-G-T

36742143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29377910-G-A

36742143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29377910-G-T

36742184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29377937-G-A

36742184-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29377937-G-T

http://identifiers.org/hco/6/GRCh38#36742212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29377965-C-A

36742212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29377965-C-T

http://identifiers.org/hco/6/GRCh38#36742263-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29377991-C-A

36742263-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29377991-C-G

36742264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29377992-A-G

36742278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 29378006-G-A

36742278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 29378006-G-T

36742321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 29378049-A-G

36742400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 29378128-G-T

36742617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29378299-T-C

36743646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 29378890-G-T

http://identifiers.org/hco/6/GRCh38#36743736-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29378973-C-A

36743736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 29378973-C-T

36743779-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29379017-G-C

36743779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29379017-G-T

36743881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29379064-T-C

http://identifiers.org/hco/6/GRCh38#36743884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29379067-C-A

36743897-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29379081-T-A

36743897-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29379081-T-G

36744126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 29379196-A-G

36744126-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 29379196-A-T

36744246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 29379273-G-A

36744246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 29379273-G-T

36744293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 29379318-G-A

36744293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 29379318-G-T

36744335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29379359-A-G

36744347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29379370-A-G

36744356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29379379-T-C

http://identifiers.org/hco/6/GRCh38#36744443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29379450-C-A

http://identifiers.org/hco/6/GRCh38#36744502-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29379498-A-C

http://identifiers.org/hco/6/GRCh38#36744549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29379532-C-A

36744558-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29379540-T-G

http://identifiers.org/hco/6/GRCh38#36744585-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29379564-A-C

36744585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29379564-A-G

36744623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29379609-G-A

36744623-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29379609-G-C

36744689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29379704-G-A

36744721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29379720-G-T

36744759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29379758-C-T

36744981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29379946-A-G

36745012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29379985-T-C

http://identifiers.org/hco/6/GRCh38#36745020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29379993-C-A

http://identifiers.org/hco/6/GRCh38#36745024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29379997-C-A

36745024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29379997-C-T

36745025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29379998-C-T

http://identifiers.org/hco/6/GRCh38#36745030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29380065-C-A

36745030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29380065-C-T

36745051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 29380087-G-A

36745051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 29380087-G-T

http://identifiers.org/hco/6/GRCh38#36745090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29380126-C-A

36745090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 29380126-C-T

36745165-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29380205-T-A

36745168-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29380208-G-C

36745168-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29380208-G-T

http://identifiers.org/hco/6/GRCh38#36745198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29380241-C-A

36745198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29380241-C-T

36745254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29380290-G-A

36745254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29380290-G-T

http://identifiers.org/hco/6/GRCh38#36745263-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29380295-C-A

36745263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29380295-C-T

36745370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29380376-G-A

36745370-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29380376-G-C

36745370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29380376-G-T

36745371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29380377-G-A

36745371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29380377-G-T

http://identifiers.org/hco/6/GRCh38#36745441-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29380446-A-C

36745441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 29380446-A-G

36745441-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 29380446-A-T

36745654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29380645-G-A

36745654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29380645-G-T

36745665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29380650-C-T

36745671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29380656-C-T

36746324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29381181-T-C

36746324-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29381181-T-G

http://identifiers.org/hco/6/GRCh38#36746510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29381341-C-A

36746510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 29381341-C-T

36746516-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 29381347-C-G

36746516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 29381347-C-T

http://identifiers.org/hco/6/GRCh38#36746657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29381457-C-A

36746657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29381457-C-T

http://identifiers.org/hco/6/GRCh38#36746725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29381523-C-A

36746725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29381523-C-T

http://identifiers.org/hco/6/GRCh38#36747037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29381829-C-A

36748104-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29383547-C-G

36748109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29383552-G-T

36748132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29383573-G-A

36748132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29383573-G-T

36748264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 29383691-G-A

36748264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 29383691-G-T

36748316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29383741-G-T

36748319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29383744-G-T

36748487-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29383904-G-C

36748495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29383909-T-C

36751423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29384625-G-A

36751466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29384662-T-C

http://identifiers.org/hco/6/GRCh38#36752476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29385294-C-A

36752476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29385294-C-T

http://identifiers.org/hco/6/GRCh38#36752481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29385299-C-A

36752481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29385299-C-T

http://identifiers.org/hco/6/GRCh38#36752620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29385336-C-A

36752620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 29385336-C-T

http://identifiers.org/hco/6/GRCh38#36752658-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29385374-A-C

http://identifiers.org/hco/6/GRCh38#36752667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29385383-C-A

36752712-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29385427-T-A

36752712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29385427-T-C

36752712-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29385427-T-G

36752743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29385454-T-C

36752762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29385474-G-A

36752762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29385474-G-T

36753147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29385795-T-C

36753192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29385827-G-A

36753192-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29385827-G-C

36753192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29385827-G-T

http://identifiers.org/hco/6/GRCh38#36753193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29385828-C-A

36753196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29385831-G-T

36753429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29386119-G-A

36753429-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29386119-G-C

36753429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29386119-G-T

http://identifiers.org/hco/6/GRCh38#36753536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29386222-C-A

36753858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29386516-C-T

36753870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29386528-A-G

36753884-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29386547-C-G

36754007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29386643-C-T

36754099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29386729-G-A

36754102-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29386732-G-C

36754123-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29386749-C-G

http://identifiers.org/hco/6/GRCh38#36754193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29386827-C-A

36754193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29386827-C-T

36754194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29386828-A-G

36754219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29386849-T-C

36754256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29386885-G-A

36754256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29386885-G-T

36754685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29386951-G-A

36754685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29386951-G-T

36754729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29386976-G-A

http://identifiers.org/hco/6/GRCh38#36754731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29386978-C-A

36754731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29386978-C-T

36754746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29386988-G-T

36754828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29387106-G-A

36754868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29387142-A-G

36754883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29387157-C-T

36754886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29387160-C-T

36754951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29387208-C-T

http://identifiers.org/hco/6/GRCh38#36754961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29387219-C-A

36754988-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29387241-G-T

36755030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29387299-T-C

36755054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29387340-G-A

36755082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29387366-G-A

36755082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29387366-G-T

36755085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29387367-T-C

http://identifiers.org/hco/6/GRCh38#36755090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29387372-C-A

36755191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29387439-A-G

36755195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29387443-C-T

36755220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29387469-G-A

36755220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29387469-G-T

http://identifiers.org/hco/6/GRCh38#36755224-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29387474-C-A

36755224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29387474-C-T

36755299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29387529-G-T

36755323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29387553-T-C

36755425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29387808-A-G

36755425-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29387808-A-T

36755428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29387811-A-G

36755593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29387939-T-C

36755752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29388081-C-T

36755772-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29388098-T-A

36755772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29388098-T-C

http://identifiers.org/hco/6/GRCh38#36755816-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29388136-A-C

36755816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29388136-A-G

36755820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29388140-G-A

36755820-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29388140-G-C

36755820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29388140-G-T

36755874-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 29388179-G-C

36755874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 29388179-G-T

http://identifiers.org/hco/6/GRCh38#36755961-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29388233-A-C

36756225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29388359-A-G

36756251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 29388385-A-G

36756356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29388478-T-C

36756407-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29388527-T-A

36756407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29388527-T-C

36756417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29388536-G-A

36756417-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29388536-G-T

36757002-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29389006-G-C

36757153-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29389157-A-T

36757164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29389195-T-C

36757165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29389196-A-G

http://identifiers.org/hco/6/GRCh38#36757166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29389197-C-A

36757166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29389197-C-T

http://identifiers.org/hco/6/GRCh38#36757381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29389460-C-A

36757404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29389482-T-C

36757485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29389562-G-T

36758884-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29389713-T-G

36758987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29389819-G-A

36759002-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29389839-C-G

36759268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29390202-G-A

36760791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29391036-T-C

36760791-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29391036-T-G

36760800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29391045-G-A

36760803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29391048-A-G

36760957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29391197-C-T

36761105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29391338-G-A

36762551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

36763079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29392463-G-A

36763079-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29392463-G-C

36763079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29392463-G-T

36763200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29392551-C-T

http://identifiers.org/hco/6/GRCh38#36763222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29392573-C-A

36764585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29394528-G-A

36765298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29395104-C-T

36765320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29395123-C-T

36765433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29395222-G-A

36765456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29395240-G-A

36765456-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29395240-G-C

36765461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29395245-A-G

36765558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29395311-G-A

36765576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29395331-C-T

36766284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29396036-G-A

36766284-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29396036-G-C

36766318-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29396070-C-G

http://identifiers.org/hco/6/GRCh38#36766380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29396135-C-A

36766380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29396135-C-T

36766410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29396158-C-T

36766441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29396194-C-T

36768022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29397867-G-A

36768053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29397890-C-T

36768158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29397987-T-C

36768846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29398280-G-T

36768882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29398315-C-T

36768883-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29398316-C-G

36769463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29398786-A-G

36769517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29398831-G-T

36769722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29399023-G-A

36769733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29399026-C-T

36770178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29399310-T-C

http://identifiers.org/hco/6/GRCh38#36770246-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29399390-A-C

36770389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29399545-A-G

36770578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29399714-C-T

36771336-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29400802-T-A

36771720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29401111-G-A

http://identifiers.org/hco/6/GRCh38#36771788-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29401133-A-C

36772003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29401307-C-T

http://identifiers.org/hco/6/GRCh38#36772384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29401506-C-A

36772424-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29401546-T-G

http://identifiers.org/hco/6/GRCh38#36772540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29401664-C-A

36772541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29401665-C-T

36772555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29401679-A-G

36773211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29401965-C-T

36773477-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29402159-A-T

36773657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29402322-A-G

36774487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29402583-G-A

36774993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 29402929-G-A

http://identifiers.org/hco/6/GRCh38#36775305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29403179-C-A

36775716-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29403501-A-T

36775914-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29404118-T-G

36775967-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29404172-T-A

36776078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29404276-C-T

36776365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29404512-C-T

36777577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29406307-G-A

36777691-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29406408-T-G

36777714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29406432-T-C

http://identifiers.org/hco/6/GRCh38#36777792-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29406500-A-C

36777792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29406500-A-G

36777796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29406511-A-G

36778153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29406780-T-C

36778153-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29406780-T-G

36778202-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29406827-C-G

36778554-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29407081-C-G

36778575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29407090-C-T

36778788-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29407217-C-G

36778788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29407217-C-T

http://identifiers.org/hco/6/GRCh38#36778789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29407218-C-A

36778789-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29407218-C-G

36778789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29407218-C-T

http://identifiers.org/hco/6/GRCh38#36778790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29407219-C-A

36778790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29407219-C-T

36778964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 29407375-G-A

36778979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29407390-G-A

36778979-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29407390-G-C

36778979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29407390-G-T

http://identifiers.org/hco/6/GRCh38#36779040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29407455-C-A

36779141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29407554-G-A

36779191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29407606-C-T

36779453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29407779-A-G

36779509-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29407834-G-C

36779659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29408013-C-T

36779738-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29408091-G-C

36779833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29408157-G-A

36779940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29408213-T-C

36780047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29408255-C-T

36780900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29408895-C-T

36780983-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29408969-T-G

36780994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29408980-C-T

36781130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29409166-G-A

36781157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29409193-C-T

36783960-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29412190-C-G

http://identifiers.org/hco/6/GRCh38#36783993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29412225-C-A

36783993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29412225-C-T

36785075-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29412930-T-A

36785075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29412930-T-C

http://identifiers.org/hco/6/GRCh38#36786346-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29414688-A-C

36786346-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29414688-A-T

36787100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29416643-G-A

36787100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29416643-G-T

36788897-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29418504-C-G

36789113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29418666-T-C

http://identifiers.org/hco/6/GRCh38#36789164-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29418717-A-C

36791502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29421073-C-T

36791506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29421077-C-T

36791838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29421342-C-T

36791934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29421427-T-C

http://identifiers.org/hco/6/GRCh38#36791944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29421436-C-A

36791944-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29421436-C-G

36791944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29421436-C-T

http://identifiers.org/hco/6/GRCh38#36792222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29421681-C-A

36792222-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29421681-C-G

36792222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29421681-C-T

36792249-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29421707-T-A

http://identifiers.org/hco/6/GRCh38#36792288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29421744-C-A

36792288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29421744-C-T

36792291-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29421747-G-C

36792291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29421747-G-T

36792570-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29421989-T-G

36792640-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29422065-G-C

36793048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29422447-G-A

36793400-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29422732-A-T

36793710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29422981-C-T

36794023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29423165-G-A

36794023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29423165-G-T

36794083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29423225-C-T

36794084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29423226-G-A

36794215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29423349-A-G

36794216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29423350-A-G

36794449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29423535-G-A

36794449-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29423535-G-T

http://identifiers.org/hco/6/GRCh38#36794460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29423546-C-A

36794460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29423546-C-T

36794540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29423616-G-A

36794540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29423616-G-T

36794541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29423617-C-T

36794604-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 29423677-T-G

36794690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29423761-A-G

36794710-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29423779-C-G

36794710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29423779-C-T

http://identifiers.org/hco/6/GRCh38#36794714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29423783-C-A

36794714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29423783-C-T

36794731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29423801-T-C

36794750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29423820-G-A

36794750-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29423820-G-C

36794750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29423820-G-T

36794885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29423899-G-A

36797318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29427870-C-T

36797711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29428047-C-T

36797894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29428223-G-A

36797938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29428267-C-T

http://identifiers.org/hco/6/GRCh38#36798183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29428416-C-A

36798183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 29428416-C-T

36798361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29428569-G-T

36798367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29428575-C-T

36798408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29428615-C-T

36798437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29428646-G-A

36798446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29428655-A-G

36798523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29428732-G-A

36798523-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29428732-G-C

36798529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29428739-G-A

36798529-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29428739-G-T

36798548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29428758-C-T

36798615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29428809-T-C

36798632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29428853-T-C

36798651-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29428874-C-G

36798651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29428874-C-T

http://identifiers.org/hco/6/GRCh38#36798693-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29428959-A-C

36798693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29428959-A-G

36798709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29429039-C-T

36798710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29429040-G-A

36798830-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29429169-C-G

36799072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29429564-C-T

36799081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29429576-C-T

36799384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29430060-T-C

36799671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29430365-T-C

36799822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29430493-T-C

36799823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29430494-T-C

36799884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29430542-T-C

36799939-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29430597-T-G

36800085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29430739-G-T

36800106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29430758-G-T

36800114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29430766-G-A

36800114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29430766-G-T

36800116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29430781-G-A

36800116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29430781-G-T

36800125-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29430790-T-G

36800133-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29430798-G-C

36800133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29430798-G-T

36800134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29430799-G-T

http://identifiers.org/hco/6/GRCh38#36800141-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29430806-A-C

36800141-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29430806-A-T

http://identifiers.org/hco/6/GRCh38#36800150-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29430815-A-C

36800150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29430815-A-G

36800150-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29430815-A-T

36800153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29430823-G-T

36800156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29430831-C-T

36800167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29430842-G-A

36800167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29430842-G-T

36800179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29430854-A-G

36800179-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29430854-A-T

36800234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29430920-G-A

36803858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29431958-C-T

36803869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29431969-G-A

36803914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29432018-T-C

36803936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29432040-A-G

36803940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29432044-C-T

36803941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29432045-C-T

36804021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29432131-G-A

36804128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29432233-G-A

http://identifiers.org/hco/6/GRCh38#36804266-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29432336-C-A

36805010-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29433015-G-C

36805119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29433158-A-G

36805428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29433442-G-A

36805430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29433444-G-A

36805492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29433517-G-T

36805514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29433538-T-C

36805578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29433588-G-A

36805646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29433623-G-A

36805989-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29433936-C-G

36810296-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29434588-G-C

36810489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29434749-G-A

36810884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29435064-C-T

36811177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29435331-C-T

36811178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29435332-G-A

36811178-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29435332-G-T

http://identifiers.org/hco/6/GRCh38#36811218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29435370-C-A

36811262-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29435414-C-G

36816247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29437482-G-A

36816332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29437568-G-A

36818029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29438632-A-G

36818029-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29438632-A-T

36818090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29438705-G-A

36819804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29440147-G-A

36819899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29440244-C-T

36819953-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29440301-T-G

36820050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29440378-C-T

36820051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29440379-G-A

36820053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29440381-C-T

36820239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29440524-C-T

36820267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29440551-A-G

36820268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29440552-G-A

36821885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29444025-T-C

36821981-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29444086-A-T

http://identifiers.org/hco/6/GRCh38#36822013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29444107-C-A

36822013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 29444107-C-T

http://identifiers.org/hco/6/GRCh38#36822109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29444160-C-A

36822109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29444160-C-T

http://identifiers.org/hco/6/GRCh38#36822275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29444294-C-A

36822275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29444294-C-T

36822330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29444347-G-A

36822535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29444624-T-C

36822539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29444628-G-A

36822582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29444715-G-A

36822889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29445009-C-T

36822936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29445052-G-A

36822936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29445052-G-T

http://identifiers.org/hco/6/GRCh38#36822949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#29445064-C-A

36822949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29445064-C-T

36822950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29445065-G-A

36822950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29445065-G-T

36823006-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29445119-G-C

36823006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29445119-G-T

36823010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29445123-T-C

http://identifiers.org/hco/6/GRCh38#36823155-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29445259-A-C

36823155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29445259-A-G

36823175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29445279-G-A

36823175-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29445279-G-T

http://identifiers.org/hco/6/GRCh38#36823202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29445305-C-A

36823202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29445305-C-T

36827055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29447676-C-T

http://identifiers.org/hco/6/GRCh38#36827151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29447770-C-A

36827151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29447770-C-T

http://identifiers.org/hco/6/GRCh38#36827240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29447849-C-A

http://identifiers.org/hco/6/GRCh38#36827244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29447853-C-A

36827244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29447853-C-T

36827327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 29447939-C-T

36827398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29447990-G-A

36827756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29448366-C-T

http://identifiers.org/hco/6/GRCh38#36834795-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29452509-A-C

http://identifiers.org/hco/6/GRCh38#36835014-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29452715-A-C

36835070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29452768-G-T

36835117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29452798-C-T

36835195-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29452871-G-C

36835203-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29452879-G-C

36835524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29453215-A-G

36835582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29453258-G-A

36835879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29453624-G-A

36836117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29453945-G-A

36836200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29454045-G-T

36836503-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29454281-T-A

36836669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29454400-G-A

36836792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29454475-C-T

36837094-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29454770-A-T

36837246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29454867-C-T

36837253-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29454878-C-G

36837330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29454939-G-A

36837595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29455094-T-C

36837642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29455140-C-T

36837878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29455317-G-A

36838133-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29455550-C-G

36838231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29455630-G-A

36838280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29455675-G-A

36838409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29455768-C-T

36838550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29455885-G-A

36838618-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29455959-T-A

36838843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29456157-G-A

36838864-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29456175-G-C

http://identifiers.org/hco/6/GRCh38#36838917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29456228-C-A

36838917-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29456228-C-G

36838936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29456247-G-A

36839148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29456448-T-C

http://identifiers.org/hco/6/GRCh38#36839165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29456464-C-A

36839165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29456464-C-T

36839243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29456538-C-T

36839259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29456563-G-A

36839259-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29456563-G-C

36839259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29456563-G-T

36839265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29456569-G-A

36839265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29456569-G-T

http://identifiers.org/hco/6/GRCh38#36839394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29456697-C-A

36839394-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29456697-C-G

36839394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2318
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29456697-C-T