155748460-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88818259-C-G

155748716-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88818004-G-C

155748764-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88817955-G-C

155749339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88817711-A-G

155749370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88817680-T-C

155749614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88817452-G-A

155749614-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88817452-G-C

155749690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88817378-A-G

155749690-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88817378-A-T

155749802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88817270-T-C

155749867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88817238-G-A

155749867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88817238-G-T

155750041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88817097-G-A

155750041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88817097-G-T

155750042-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88817096-G-C

155750409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88816796-G-T

155750514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88816742-G-A

155750514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88816742-G-T

155750524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88816736-C-T

155750683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88816593-T-C

155750683-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88816593-T-G

155751743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88816126-G-A

155751743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88816126-G-T

http://identifiers.org/hco/1/GRCh38#155751924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88815944-C-A

155751924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88815944-C-T

155752122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88815753-G-A

155752147-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88815728-C-G

155752147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88815728-C-T

http://identifiers.org/hco/1/GRCh38#155752159-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88815716-A-C

155752159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88815716-A-G

http://identifiers.org/hco/1/GRCh38#155752289-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88815589-A-C

155752289-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: synonymous variant
orthologous variants: 88815589-A-T

155752291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: missense variant
orthologous variants: 88815587-G-A

155752291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: missense variant
orthologous variants: 88815587-G-T

155752377-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: missense variant
orthologous variants: 88815501-C-G

155752377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: missense variant
orthologous variants: 88815501-C-T

http://identifiers.org/hco/1/GRCh38#155752577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88815304-C-A

155752577-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: synonymous variant
orthologous variants: 88815304-C-G

155753082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron variant
orthologous variants: 88815006-A-G

155753089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron variant
orthologous variants: 88814999-G-A

155753089-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron variant
orthologous variants: 88814999-G-C

155753089-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron variant
orthologous variants: 88814999-G-T

155753133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron variant
orthologous variants: 88814958-T-C

155753133-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron variant
orthologous variants: 88814958-T-G

155753185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron variant
orthologous variants: 88814906-G-T

155753186-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron variant
orthologous variants: 88814905-C-G

155753186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron variant
orthologous variants: 88814905-C-T

155753208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: synonymous variant
orthologous variants: 88814883-A-G

155753209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: missense variant
orthologous variants: 88814882-A-G

155753432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron variant
orthologous variants: 88814661-C-T

155754292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88813055-G-T

155754321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88813025-C-T

155754361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88812881-G-T

155754454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88812791-G-T

155754507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88812738-T-C

155757228-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88810157-C-G

http://identifiers.org/hco/1/GRCh38#155757363-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88810022-C-A

155757376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88810002-C-T

155757876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88809038-G-T

155758132-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron variant
orthologous variants: 88808782-G-C

155758263-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron variant
orthologous variants: 88808630-G-C

155760348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron variant
orthologous variants: 88807531-A-G

155760348-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron variant
orthologous variants: 88807531-A-T

http://identifiers.org/hco/1/GRCh38#155760358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88807521-C-A

155760358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron variant
orthologous variants: 88807521-C-T

155760405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron variant
orthologous variants: 88807475-C-T

http://identifiers.org/hco/1/GRCh38#155760432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88807450-C-A

155760432-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron variant
orthologous variants: 88807450-C-G

http://identifiers.org/hco/1/GRCh38#155760433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88807449-C-A

155760433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron variant
orthologous variants: 88807449-C-T

155760670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron variant
orthologous variants: 88807207-A-G

155760674-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron variant
orthologous variants: 88807203-T-A

155760674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron variant
orthologous variants: 88807203-T-C

http://identifiers.org/hco/1/GRCh38#155760694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88807180-C-A

155760694-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron variant
orthologous variants: 88807180-C-G

155760696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron variant
orthologous variants: 88807178-A-G

155760731-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron variant
orthologous variants: 88807150-G-C

155760731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron variant
orthologous variants: 88807150-G-T

http://identifiers.org/hco/1/GRCh38#155760753-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88807129-C-A

155760766-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron variant
orthologous variants: 88807117-T-G

155760832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron variant
orthologous variants: 88807065-T-C

155760834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron variant
orthologous variants: 88807063-C-T

155760968-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron variant
orthologous variants: 88806970-T-G

155760972-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron variant
orthologous variants: 88806966-T-G

155760994-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron variant
orthologous variants: 88806946-C-G

155760994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron variant
orthologous variants: 88806946-C-T

155761063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron variant
orthologous variants: 88806878-T-C

155761876-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron variant
orthologous variants: 88806755-G-C

155761891-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron variant
orthologous variants: 88806740-C-G

155761960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron variant
orthologous variants: 88806679-T-C

155761974-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron variant
orthologous variants: 88806665-A-T

155762111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron variant
orthologous variants: 88806454-T-C

155762132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron variant
orthologous variants: 88806433-T-C

http://identifiers.org/hco/1/GRCh38#155762151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88806414-C-A

155762170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron variant
orthologous variants: 88806401-A-G

155762398-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron variant
orthologous variants: 88806174-T-A

155762398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron variant
orthologous variants: 88806174-T-C

155762441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron variant
orthologous variants: 88806139-A-G

155762443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron variant
orthologous variants: 88806137-G-A

155762443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron variant
orthologous variants: 88806137-G-T

155762483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron variant
orthologous variants: 88806099-T-C

http://identifiers.org/hco/1/GRCh38#155763243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88805713-C-A

155763259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron variant
orthologous variants: 88805698-A-G

155763420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: missense_variant, undefined
orthologous variants: 88805554-T-C

155763479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: missense_variant, undefined
orthologous variants: 88805495-T-C

155763522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: missense_variant, undefined
orthologous variants: 88805452-T-C

155763522-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: missense_variant, undefined
orthologous variants: 88805452-T-G

155763523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: synonymous_variant, undefined
orthologous variants: 88805451-G-A

155763547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: synonymous_variant, undefined
orthologous variants: 88805427-C-T

155764777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 88804061-G-A

155764777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 88804061-G-T

155764791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88804047-T-C

155764791-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88804047-T-G

http://identifiers.org/hco/1/GRCh38#155764794-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88804044-A-C

155764794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88804044-A-G

http://identifiers.org/hco/1/GRCh38#155764797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88804041-C-A

155764797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88804041-C-T

155764800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88804038-G-T

155764902-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88803945-G-C

155764902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88803945-G-T

155765093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88803783-C-T

http://identifiers.org/hco/1/GRCh38#155765157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88803719-C-A

155765157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88803719-C-T

155765167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88803709-T-C

155765355-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88803527-T-G

155765392-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88803490-G-C

http://identifiers.org/hco/1/GRCh38#155765417-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88803465-A-C

155765417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88803465-A-G

155765456-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88803426-G-C

155765457-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88803425-G-C

155765457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88803425-G-T

155765522-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88803357-G-C

155765522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88803357-G-T

155765580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88803302-C-T

155765617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88803265-T-C

155765967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88802870-G-A

155765967-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88802870-G-C

http://identifiers.org/hco/1/GRCh38#155766014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88802823-C-A

155766055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88802782-G-A

155766091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88802749-A-G

http://identifiers.org/hco/1/GRCh38#155766122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88802718-C-A

155766147-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88802693-T-A

155766185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88802655-A-G

155766202-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88802638-A-T

155766226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88802614-A-G

155766247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88802587-G-A

155766247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88802587-G-T

http://identifiers.org/hco/1/GRCh38#155766289-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/3/GRCm39#88802545-C-A

155766314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88802520-T-C

155766326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88802508-T-C

155766342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88802492-T-C

155766344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88802490-T-C

155766360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88802474-C-T

155766394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88802440-G-A

155766394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88802440-G-T

155766404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88802430-G-A

155766404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88802430-G-T

155766483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88802351-C-T

155766577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88802257-C-T

155766580-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88802254-T-A

155766671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88802163-C-T

155767396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88801890-C-T

155767622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88801685-T-C

155767622-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88801685-T-G

155767653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88801680-A-G

155767820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88801503-G-A

155770586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88800450-T-C

155770678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88800339-A-G

155770678-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88800339-A-T

155770687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88800330-G-A

155770904-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88800098-A-T

http://identifiers.org/hco/1/GRCh38#155771085-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88799955-A-C

http://identifiers.org/hco/1/GRCh38#155771116-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88799924-A-C

155771129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88799911-G-T

155771176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88799864-A-G

155772934-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88798376-A-T

155772937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88798373-T-C

155773229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88798099-C-T

155773357-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88798004-T-A

155773376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88797986-A-G

155773376-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88797986-A-T

155773381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88797983-A-G

http://identifiers.org/hco/1/GRCh38#155773414-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88797962-A-C

155773414-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88797962-A-T

http://identifiers.org/hco/1/GRCh38#155773442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88797930-C-A

155773442-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88797930-C-G

155773442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88797930-C-T

155774865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88797263-T-C

155774865-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88797263-T-G

http://identifiers.org/hco/1/GRCh38#155774923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88797206-C-A

155775217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88796932-A-G

155775229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88796916-T-C

155775271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88796874-G-T

http://identifiers.org/hco/1/GRCh38#155776259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88795087-C-A

155776259-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88795087-C-G

155776259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88795087-C-T

155776300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88795039-T-C

http://identifiers.org/hco/1/GRCh38#155776303-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88795036-A-C

155776304-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88795035-T-A

155776319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88795020-G-T

155776377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88794968-G-T

155776378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88794967-G-T

155776513-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88794838-T-A

155777837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88794194-G-T

http://identifiers.org/hco/1/GRCh38#155777927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88794115-C-A

155777927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88794115-C-T

155778025-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88793952-T-G

155783681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88787775-T-C

155783731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88787725-T-C

155783731-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88787725-T-G

155785183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88777277-T-C

155785245-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88777231-C-G

155785245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88777231-C-T

155785253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88777223-A-G

155785259-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88777217-A-T

155785384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88777098-A-G

155785438-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88777043-A-T

155785443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88777038-G-A

155785443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88777038-G-T

http://identifiers.org/hco/1/GRCh38#155785445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88777036-C-A

155785445-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88777036-C-G

155785445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88777036-C-T

155794777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88776414-C-T

155794845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88776331-C-T

155794910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88776272-A-G

155794986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88776204-A-G

155795085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88776121-T-C

155795111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88776095-C-T

http://identifiers.org/hco/1/GRCh38#155795187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88776019-C-A

155804913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88770959-G-A

155804913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88770959-G-T

155804945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88770921-T-C

155805182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88770679-T-C

155805197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88770663-T-C

155813170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88766769-A-G

http://identifiers.org/hco/1/GRCh38#155813504-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88766503-A-C

155813504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88766503-A-G

155813581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88766415-C-T

155813593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88766403-T-C

155813824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88766174-G-A

155813824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88766174-G-T

155813894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88766144-G-A

155813894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88766144-G-T

155814230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88765904-G-A

155814230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88765904-G-T

155814283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88765853-A-G

155814317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88765823-G-A

155814317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88765823-G-T

155814972-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88765167-G-C

155815072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88765086-C-T

155815145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88765065-T-C

155815327-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88764967-G-C

155815736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88764608-G-A

155815736-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88764608-G-T

155815775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88764571-G-A

155815775-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88764571-G-C

155815775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88764571-G-T

155815795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88764541-A-G

155815916-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88764372-T-A

155815971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88764100-G-A

http://identifiers.org/hco/1/GRCh38#155815983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88764088-C-A

155815983-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88764088-C-G

http://identifiers.org/hco/1/GRCh38#155816099-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88763891-A-C

155816099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88763891-A-G

155816280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88763707-A-G

155816280-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88763707-A-T

http://identifiers.org/hco/1/GRCh38#155816342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88763666-C-A

155816342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88763666-C-T

155816353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88763655-A-G

155816378-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88763630-C-G

155820519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88763252-A-G

155820575-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88763189-A-T

http://identifiers.org/hco/1/GRCh38#155821381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88763065-C-A

155821390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88763056-A-G

155821475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 88763004-A-G

155821588-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88762888-T-G

155821597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88762879-G-T

155821678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88762797-G-A

155821678-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88762797-G-C

155821678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88762797-G-T

155821786-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88762527-T-G

155821935-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88762352-A-T

155822061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88762286-A-G

155822162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88762212-T-C

155822201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88762174-A-G

155822201-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88762174-A-T

155822413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88761970-C-T

155822483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 88761900-A-G

155822489-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88761891-C-G

155826803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88753914-G-T

155826842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88753879-G-A

155826842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88753879-G-T

155827039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88753682-C-T

155827117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88753600-G-A

155827117-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88753600-G-C

155827117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88753600-G-T

http://identifiers.org/hco/1/GRCh38#155827166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88753555-C-A

155832686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88747620-T-C

155832707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88747597-T-C

http://identifiers.org/hco/1/GRCh38#155832709-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88747595-A-C

155832727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88747580-T-C

155851376-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88746053-C-G

155851414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88746015-A-G

http://identifiers.org/hco/1/GRCh38#155852193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88745968-C-A

http://identifiers.org/hco/1/GRCh38#155852213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88745948-C-A

155852237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88745928-C-T

155852370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88745813-C-T

155852871-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88745289-G-C

155852876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88745284-G-T

155852911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88745229-G-A

155852911-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88745229-G-C

155853393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88744708-T-C

155853530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88744571-G-A

155853745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88744356-T-C

155853808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 88744293-T-C

155853882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88744214-A-G

http://identifiers.org/hco/1/GRCh38#155853915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88744181-C-A

155853915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88744181-C-T

http://identifiers.org/hco/1/GRCh38#155857014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#88742741-C-A

155857014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88742741-C-T

http://identifiers.org/hco/1/GRCh38#155857026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#88742729-C-A

155857026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88742729-C-T

155857116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88742631-C-T

155857168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88742578-T-C

155857168-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88742578-T-G

155857237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88742507-G-A

http://identifiers.org/hco/1/GRCh38#155857241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#88742503-C-A

155857241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88742503-C-T

http://identifiers.org/hco/1/GRCh38#155857248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#88742496-C-A

155857248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88742496-C-T

155857260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88742493-G-A

155857260-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88742493-G-T

155857261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88742492-T-C

155857261-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88742492-T-G

155857267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 88742486-A-G

http://identifiers.org/hco/1/GRCh38#155857285-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#88742468-A-C

155857285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88742468-A-G

155857287-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88742466-T-A

155857287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 88742466-T-C

155857311-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, undefined
orthologous variants: 88742442-G-C

155857311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, undefined
orthologous variants: 88742442-G-T

155857325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, undefined
orthologous variants: 88742428-C-T

155857496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, undefined
orthologous variants: 88742326-G-A

155857524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron_variant, undefined
orthologous variants: 88742318-G-A

155858155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: intron variant
orthologous variants: 88741560-A-G

155859360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25973
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 88739942-T-C