57883613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: 3 prime UTR variant
orthologous variants: 95967402-C-T

http://identifiers.org/hco/16/GRCh38#57883676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95967451-C-A

57883764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: 3 prime UTR variant
orthologous variants: 95967524-G-A

57883764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: 3 prime UTR variant
orthologous variants: 95967524-G-T

57883765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: 3 prime UTR variant
orthologous variants: 95967525-G-A

57883779-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: 3 prime UTR variant
orthologous variants: 95967537-T-G

http://identifiers.org/hco/16/GRCh38#57883789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95967547-C-A

57883827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: 3 prime UTR variant
orthologous variants: 95967586-T-C

57883899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: 3 prime UTR variant
orthologous variants: 95967657-A-G

57884005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: 3 prime UTR variant
orthologous variants: 95967764-G-A

57884005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: 3 prime UTR variant
orthologous variants: 95967764-G-T

http://identifiers.org/hco/16/GRCh38#57884170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95967828-C-A

57884170-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: synonymous variant
orthologous variants: 95967828-C-G

57884170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: synonymous variant
orthologous variants: 95967828-C-T

http://identifiers.org/hco/16/GRCh38#57884317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95967972-C-A

57884317-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: synonymous variant
orthologous variants: 95967972-C-G

57884317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: synonymous variant
orthologous variants: 95967972-C-T

57884359-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: synonymous variant
orthologous variants: 95968017-C-G

57884359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: synonymous variant
orthologous variants: 95968017-C-T

57884365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: synonymous variant
orthologous variants: 95968023-C-T

57884393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: missense_variant, stop_gained
orthologous variants: 95968047-G-A

57884393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: missense variant
orthologous variants: 95968047-G-T

57884601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95968243-G-A

57884601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95968243-G-T

57887701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95968671-A-G

57887713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95968683-G-A

57887713-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95968683-G-C

57887713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95968683-G-T

57887848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 95968810-A-G

57887848-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 95968810-A-T

57888097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95969059-G-T

57888159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95969130-A-G

http://identifiers.org/hco/16/GRCh38#57888335-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95969279-A-C

57889947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95969598-C-T

57890059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95969710-G-A

57890333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95969989-A-G

57890340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95969996-G-A

57890381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95970045-T-C

57890471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95970114-T-C

57893965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95971752-T-C

57894065-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95971848-T-G

57894094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95971880-C-T

57894095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95971881-G-A

57894097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95971883-T-C

http://identifiers.org/hco/16/GRCh38#57897510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95975115-C-A

57897510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: synonymous variant
orthologous variants: 95975115-C-T

57897525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: synonymous variant
orthologous variants: 95975130-G-A

57897525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: synonymous variant
orthologous variants: 95975130-G-T

57897617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95975253-T-C

57897646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95975306-G-A

57897691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95975368-G-A

57897691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95975368-G-T

57897777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95975527-T-C

57897780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95975531-C-T

57897787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95975538-G-T

http://identifiers.org/hco/16/GRCh38#57897819-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95975570-A-C

57897819-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: synonymous variant
orthologous variants: 95975570-A-T

57899709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95976554-C-T

http://identifiers.org/hco/16/GRCh38#57899756-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#95976598-A-C

57899907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 95976685-C-T

57899936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 95976709-A-G

57899977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95976718-A-G

57900015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95976755-C-T

57900213-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95976885-C-G

57900924-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95978300-T-A

57901138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95978458-A-G

57901382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 95978563-G-T

57901409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 95978590-G-A

57901497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95978678-G-A

57901497-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95978678-G-C

http://identifiers.org/hco/16/GRCh38#57901687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95978867-C-A

57901687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95978867-C-T

57901693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95978873-A-G

57901844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95979001-A-G

http://identifiers.org/hco/16/GRCh38#57903690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95979767-C-A

57903690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95979767-C-T

57903763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95979819-G-T

57903808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95979862-C-T

http://identifiers.org/hco/16/GRCh38#57903835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95979890-C-A

57903835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 95979890-C-T

57903967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 95980022-T-C

57903990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 95980050-A-G

57904028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95980088-G-A

57904028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95980088-G-T

57904042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95980095-C-T

http://identifiers.org/hco/16/GRCh38#57904075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95980126-C-A

57904075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95980126-C-T

57904086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95980137-G-A

57904086-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95980137-G-T

57904095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95980143-A-G

57904119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95980167-G-A

57904119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95980167-G-T

http://identifiers.org/hco/16/GRCh38#57904125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95980173-C-A

57904125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95980173-C-T

57904214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95980226-T-C

57904600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95980573-T-C

57904650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95980617-G-A

57904651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95980618-G-A

57904651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95980618-G-T

57904665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95980628-A-G

57904680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95980643-G-A

57904767-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 95980723-C-G

57904767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 95980723-C-T

57904895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95980850-G-A

57904937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95980892-G-A

57904937-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95980892-G-C

57905009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95980932-G-A

57911600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95984316-T-C

57911608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95984324-C-T

http://identifiers.org/hco/16/GRCh38#57911613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95984329-C-A

57911613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95984329-C-T

http://identifiers.org/hco/16/GRCh38#57911614-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95984330-A-C

57911614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95984330-A-G

57911622-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95984337-G-T

57911631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95984346-G-T

http://identifiers.org/hco/16/GRCh38#57911644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95984359-C-A

57911653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95984368-A-G

57911678-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95984394-G-C

57911731-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95984446-C-G

57911735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95984450-G-T

57911747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95984459-G-A

57912015-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95985176-T-G

57912016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95985177-G-A

57912016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95985177-G-T

http://identifiers.org/hco/16/GRCh38#57912039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95985201-C-A

57912121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95985272-T-C

57912166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95985316-T-C

57912401-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95985515-C-G

57912826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95985676-G-A

57912826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95985676-G-T

57912831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95985681-T-C

57912831-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95985681-T-G

57912903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95985736-T-C

57913018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95985847-A-G

57914560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95986027-G-A

57914894-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95986372-G-C

57915117-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95986630-T-A

57915117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95986630-T-C

57915216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95986708-G-A

57915216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95986708-G-T

http://identifiers.org/hco/16/GRCh38#57915355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95986842-C-A

http://identifiers.org/hco/16/GRCh38#57915356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95986843-C-A

57915356-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95986843-C-G

57915356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95986843-C-T

57915358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95986845-T-C

57915360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95986847-G-T

57915380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95986867-A-G

57915412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95986892-T-C

57915436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95986913-G-A

57915436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95986913-G-T

http://identifiers.org/hco/16/GRCh38#57915486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95986962-C-A

57915486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95986962-C-T

57915558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95987033-G-T

57915982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95987121-T-C

http://identifiers.org/hco/16/GRCh38#57915996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95987135-C-A

57915996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95987135-C-T

57916028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95987173-G-A

57916028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95987173-G-T

57916065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95987209-G-A

57916073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95987217-G-A

57916096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95987240-G-A

57916096-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95987240-G-T

57916159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: synonymous variant
orthologous variants: 95987282-T-C

57916159-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: synonymous variant
orthologous variants: 95987282-T-G

57916230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95987341-G-T

57916249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95987356-G-T

57916254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95987361-T-C

57916254-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95987361-T-G

http://identifiers.org/hco/16/GRCh38#57916290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95987381-C-A

57916290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95987381-C-T

http://identifiers.org/hco/16/GRCh38#57916293-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95987384-A-C

57916293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95987384-A-G

http://identifiers.org/hco/16/GRCh38#57916294-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95987385-A-C

57916294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95987385-A-G

57916310-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95987386-T-G

57916313-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95987389-T-A

57916313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95987389-T-C

57916321-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95987397-T-A

57916321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95987397-T-C

57916331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95987406-T-C

57916331-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95987406-T-G

http://identifiers.org/hco/16/GRCh38#57916340-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95987415-A-C

57916428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95987513-T-C

57916437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95987522-C-T

57916514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95987594-G-A

57916738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95989249-C-T

http://identifiers.org/hco/16/GRCh38#57916774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95989260-C-A

57916903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95989362-G-A

http://identifiers.org/hco/16/GRCh38#57917123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#95989568-C-A

http://identifiers.org/hco/16/GRCh38#57917144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95989595-C-A

57917144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95989595-C-T

57917223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95989672-G-A

57917234-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, undefined
orthologous variants: 95989683-C-G

http://identifiers.org/hco/16/GRCh38#57917251-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#95989700-A-C

57917295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: synonymous_variant, undefined
orthologous variants: 95989744-C-T

57917340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: synonymous variant
orthologous variants: 95989789-G-A

57917340-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: missense variant
orthologous variants: 95989789-G-C

57917391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: synonymous_variant, undefined
orthologous variants: 95989840-G-A

57917497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95989945-G-A

57917497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95989945-G-T

57917612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95989987-G-A

57917612-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95989987-G-C

57917618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95989993-G-A

57917618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95989993-G-T

http://identifiers.org/hco/16/GRCh38#57917626-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95990001-A-C

57917626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95990001-A-G

57917626-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95990001-A-T

http://identifiers.org/hco/16/GRCh38#57917792-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95990150-A-C

http://identifiers.org/hco/16/GRCh38#57918326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95990493-C-A

57918326-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95990493-C-G

57918326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95990493-C-T

57918438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95990616-A-G

http://identifiers.org/hco/16/GRCh38#57918443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95990621-C-A

57918591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95990785-G-A

57918661-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95990844-T-A

57918666-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95990849-A-T

57919074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95990992-G-A

57919075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95990993-G-A

57919075-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95990993-G-C

57919077-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95990995-A-T

57919211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: synonymous variant
orthologous variants: 95991128-G-A

57919260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 95991178-G-A

57919281-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95991199-G-C

57919352-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95991251-G-C

57919395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95991295-G-T

57919561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95991502-G-A

http://identifiers.org/hco/16/GRCh38#57919659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95991603-C-A

57919883-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95991798-G-C

http://identifiers.org/hco/16/GRCh38#57919956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95991979-C-A

57919956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95991979-C-T

57920176-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95992401-G-C

57920264-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95992464-T-A

57920302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95992500-G-A

57920302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95992500-G-T

57920304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95992502-C-T

http://identifiers.org/hco/16/GRCh38#57920330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95992519-C-A

http://identifiers.org/hco/16/GRCh38#57920347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95992543-C-A

57920453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: missense variant
orthologous variants: 95992648-T-C

57920523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: synonymous variant
orthologous variants: 95992718-G-A

57920662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95992853-C-T

57921681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95992890-C-T

57921721-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95992931-C-G

57921721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95992931-C-T

57921803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95993010-C-T

57921848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95993060-T-C

57921951-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95993165-G-C

57921986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95993199-A-G

57922287-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95993474-C-G

57922851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95993900-G-A

57923003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95994001-A-G

57923047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95994050-G-A

http://identifiers.org/hco/16/GRCh38#57923057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95994059-C-A

57923057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95994059-C-T

57923103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 95994108-G-T

http://identifiers.org/hco/16/GRCh38#57923141-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95994147-A-C

57923141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 95994147-A-G

57923162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 95994163-G-A

57923162-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 95994163-G-C

57923162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 95994163-G-T

http://identifiers.org/hco/16/GRCh38#57923185-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95994183-A-C

57923185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 95994183-A-G

http://identifiers.org/hco/16/GRCh38#57923211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95994202-C-A

57923211-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 95994202-C-G

57923211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 95994202-C-T

http://identifiers.org/hco/16/GRCh38#57923216-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95994207-A-C

57923216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 95994207-A-G

57923216-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 95994207-A-T

57923368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 95994371-G-T

57923481-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95994463-T-A

http://identifiers.org/hco/16/GRCh38#57923745-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95994647-A-C

57923890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95994780-G-A

57923952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95994834-G-A

57924030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95994901-G-A

57924182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95994994-A-G

57924242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95995054-G-A

57924242-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95995054-G-T

57924346-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95995143-C-G

57924501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95995549-T-C

http://identifiers.org/hco/16/GRCh38#57925383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95995976-C-A

57925383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95995976-C-T

57925384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95995977-T-C

57925456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95996052-A-G

57925548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95996726-C-T

57925625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95996802-A-G

57931673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95997388-G-A

57931673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95997388-G-T

57931757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 95997472-T-C

57931817-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 95997532-G-C

57931817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 95997532-G-T

57931949-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95997635-C-G

57931949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95997635-C-T

http://identifiers.org/hco/16/GRCh38#57931997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95997647-C-A

http://identifiers.org/hco/16/GRCh38#57932004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95997654-C-A

http://identifiers.org/hco/16/GRCh38#57932012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95997662-C-A

57932071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95997702-T-C

57932083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95997723-G-A

http://identifiers.org/hco/16/GRCh38#57937005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96002095-C-A

57937005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96002095-C-T

57937063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96002156-A-G

57937095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 96002187-G-T

57937146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 96002238-T-C

57937259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 96002351-G-A

57937259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 96002351-G-T

57937328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 96002420-G-A

57937328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 96002420-G-T

57937357-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 96002449-G-C

57937362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 96002454-G-A

57937362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 96002454-G-T

57937438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96002608-T-C

57937458-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96002627-C-G

57937458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96002627-C-T

57937491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96002660-G-A

57937546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96002715-C-T

57937756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96002883-C-T

57937825-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96002944-G-C

57937915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96002974-C-T

57938042-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96003071-G-C

57938192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96003166-G-A

57938519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96003324-G-A

57938519-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96003324-G-C

57939278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96004254-G-A

57939278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96004254-G-T

57939279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96004255-G-T

57939284-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96004260-T-A

57939307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96004280-G-A

57939307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96004280-G-T

57939314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96004287-G-A

57939314-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96004287-G-C

57939314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96004287-G-T

57939337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96004310-G-A

57939337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96004310-G-T

57939510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 96004422-T-C

57939538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 96004450-T-C

57939545-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 96004457-C-G

57939700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96004555-C-T

http://identifiers.org/hco/16/GRCh38#57939718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96004573-C-A

57939742-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96004583-T-G

57939961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96004701-C-T

http://identifiers.org/hco/16/GRCh38#57940103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96004788-C-A

57940103-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96004788-C-G

57940103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96004788-C-T

57940129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96004814-C-T

57940208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96004853-G-A

57940208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96004853-G-T

http://identifiers.org/hco/16/GRCh38#57940255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96004889-C-A

57940255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 96004889-C-T

http://identifiers.org/hco/16/GRCh38#57940263-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96004897-C-A

57940263-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 96004897-C-G

57940263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 96004897-C-T

57940418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96005043-G-A

57940418-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96005043-G-T

57940419-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96005044-G-C

http://identifiers.org/hco/16/GRCh38#57940436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96005061-C-A

57940436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96005061-C-T

http://identifiers.org/hco/16/GRCh38#57940489-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96005090-A-C

57940653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96005225-C-T

57940830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96005466-C-T

http://identifiers.org/hco/16/GRCh38#57940896-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96005537-C-A

http://identifiers.org/hco/16/GRCh38#57940902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96005543-C-A

57940922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96005565-T-C

57940955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96005606-G-A

57940980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96005631-T-C

57941066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96005713-A-G

57941079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96005726-G-A

57941278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96006333-C-T

57941370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96006393-G-A

57941370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96006393-G-T

57941489-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96006504-A-T

57941494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96006509-G-A

57945587-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96007331-T-A

57945587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96007331-T-C

57945605-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96007346-A-T

57945884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, undefined
orthologous variants: 96007601-A-G

http://identifiers.org/hco/16/GRCh38#57945902-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#96007623-A-C

57945964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96007663-T-C

57945987-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96007685-G-C

http://identifiers.org/hco/16/GRCh38#57946059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96007753-C-A

http://identifiers.org/hco/16/GRCh38#57946268-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96007926-C-A

57946268-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96007926-C-G

57946268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96007926-C-T

57946300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96007959-T-C

57946351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96008010-G-A

57946374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96008034-A-G

http://identifiers.org/hco/16/GRCh38#57946398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96008058-C-A

57946398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 96008058-C-T

57946451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 96008111-T-C

57946469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 96008129-G-A

57946469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 96008129-G-T

57946568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 96008254-A-G

57946585-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 96008270-T-G

57946677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96008362-G-A

57946677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96008362-G-T

http://identifiers.org/hco/16/GRCh38#57946680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96008363-C-A

57946680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96008363-C-T

57946695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96008379-A-G

57947093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96008723-G-A

57947210-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96008799-T-G

http://identifiers.org/hco/16/GRCh38#57947738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96009442-C-A

57947777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96009481-G-A

57947820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96009523-C-T

57947826-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96009529-T-A

57947828-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96009531-A-T

57947868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96009560-A-G

http://identifiers.org/hco/16/GRCh38#57948178-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96009847-A-C

57950294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96013152-G-A

57950294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96013152-G-T

http://identifiers.org/hco/16/GRCh38#57950318-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96013178-A-C

57950318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96013178-A-G

57950342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96013194-A-G

http://identifiers.org/hco/16/GRCh38#57950349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96013201-C-A

57950349-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96013201-C-G

57950355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96013207-T-C

57950467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: synonymous variant
orthologous variants: 96013318-G-A

http://identifiers.org/hco/16/GRCh38#57950607-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96013453-C-A

57950607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96013453-C-T

57950822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96013658-G-A

57950916-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96013746-G-C

57950925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96013755-C-T

57950987-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96013818-G-C

57951014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96013845-G-A

57951014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96013845-G-T

57951314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96014484-G-A

57951512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96014642-T-C

57951648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96014745-G-A

57951747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96014840-C-T

57951819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96014910-C-T

http://identifiers.org/hco/16/GRCh38#57951908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96014967-C-A

57951976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96015034-T-C

57951989-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96015047-G-C

57952268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96015239-A-G

57952383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96015325-C-T

57952384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96015326-G-A

http://identifiers.org/hco/16/GRCh38#57952483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96015413-C-A

57953553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96015810-A-G

57953856-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96016089-C-G

57953856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96016089-C-T

http://identifiers.org/hco/16/GRCh38#57954097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96016268-C-A

57954198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96016384-T-C

57954579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96017015-A-G

57954595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96017027-G-A

57954595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96017027-G-T

57954600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96017032-T-C

57954756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 96017296-G-T

http://identifiers.org/hco/16/GRCh38#57954863-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96017379-A-C

57954878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 96017395-C-T

57954960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 96017421-G-A

57954960-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 96017421-G-C

57954960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 96017421-G-T

http://identifiers.org/hco/16/GRCh38#57955038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96017452-C-A

57955038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 96017452-C-T

57955159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 96017511-G-A

57955159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 96017511-G-T

57955160-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 96017512-G-T

57955175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 96017527-G-A

57955175-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 96017527-G-C

57955175-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 96017527-G-T

57955265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 96017606-G-A

57955265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 96017606-G-T

57955424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96017847-G-A

57955432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96017855-G-A

57955432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96017855-G-T

57955439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96017862-A-G

57955439-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96017862-A-T

57955440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96017863-G-T

57955518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96018098-G-A

57955650-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96018228-T-A

57955650-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96018228-T-G

57955659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96018237-G-A

57955811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96018309-G-A

57955811-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96018309-G-C

57955849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96018383-C-T

57955868-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96018402-G-C

57956123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96018610-G-T

57956199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96018704-G-T

57956293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96018804-G-T

57956362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96019359-A-G

http://identifiers.org/hco/16/GRCh38#57956489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96019460-C-A

57956493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96019462-C-T

57956494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96019463-G-A

57956523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96019492-C-T

57956532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96019496-G-A

57956662-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96019605-T-A

57956662-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96019605-T-G

57957002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96019942-G-A

57957186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96020075-G-T

57957209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96020098-G-T

57957366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: synonymous variant
orthologous variants: 96020209-G-A

http://identifiers.org/hco/16/GRCh38#57957432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96020313-C-A

57957432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96020313-C-T

http://identifiers.org/hco/16/GRCh38#57957447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96020328-C-A

57957447-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96020328-C-G

57957447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96020328-C-T

57957458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, undefined
orthologous variants: 96020339-G-A

57957458-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, undefined
orthologous variants: 96020339-G-C

57957458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, undefined
orthologous variants: 96020339-G-T

http://identifiers.org/hco/16/GRCh38#57957461-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#96020341-A-C

57957872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96021064-C-T

57958047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96021376-G-A

http://identifiers.org/hco/16/GRCh38#57958322-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96021651-A-C

57958322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96021651-A-G

57958322-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96021651-A-T

http://identifiers.org/hco/16/GRCh38#57958332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96021666-C-A

57958332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96021666-C-T

http://identifiers.org/hco/16/GRCh38#57958346-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96021679-A-C

57958346-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96021679-A-T

http://identifiers.org/hco/16/GRCh38#57958362-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96021695-C-A

57958460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: synonymous variant
orthologous variants: 96021798-G-A

57958519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96021854-G-T

57958545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96021869-T-C

http://identifiers.org/hco/16/GRCh38#57958561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96021878-C-A

57958561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96021878-C-T

http://identifiers.org/hco/16/GRCh38#57958593-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96021908-A-C

57958596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96021911-C-T

http://identifiers.org/hco/16/GRCh38#57958600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96021915-C-A

57958601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96021916-A-G

57958601-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96021916-A-T

http://identifiers.org/hco/16/GRCh38#57958626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96021940-C-A

57958626-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96021940-C-G

57958646-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96021960-C-G

57958646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96021960-C-T

57958718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96022041-C-T

57958724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96022047-T-C

57958725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96022048-T-C

http://identifiers.org/hco/16/GRCh38#57958726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96022049-C-A

57958726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96022049-C-T

57958741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96022064-A-G

57959737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96023006-A-G

57959739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96023008-G-T

57959757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96023026-G-A

57959757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96023026-G-T

57959769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96023038-A-G

57959784-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96023052-T-A

57959784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96023052-T-C

57959784-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96023052-T-G

http://identifiers.org/hco/16/GRCh38#57959798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96023064-C-A

57959798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96023064-C-T

http://identifiers.org/hco/16/GRCh38#57959892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96023159-C-A

57959892-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: missense variant
orthologous variants: 96023159-C-G

57959892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: missense variant
orthologous variants: 96023159-C-T

57959893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: synonymous variant
orthologous variants: 96023160-A-G

57959935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: synonymous variant
orthologous variants: 96023196-G-A

57959935-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: synonymous variant
orthologous variants: 96023196-G-C

57959935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: synonymous variant
orthologous variants: 96023196-G-T

57959939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: missense variant
orthologous variants: 96023200-G-A

57959939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: missense variant
orthologous variants: 96023200-G-T

http://identifiers.org/hco/16/GRCh38#57959986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96023235-C-A

57959986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: synonymous variant
orthologous variants: 96023235-C-T

57960041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: missense variant
orthologous variants: 96023278-A-G

http://identifiers.org/hco/16/GRCh38#57960089-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96023325-C-A

57960089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96023325-C-T

57960136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96023373-G-A

57960136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96023373-G-T

http://identifiers.org/hco/16/GRCh38#57960154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96023391-C-A

57960154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96023391-C-T

57960169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96023406-G-A

57960169-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96023406-G-C

57960169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96023406-G-T

http://identifiers.org/hco/16/GRCh38#57960176-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96023413-C-A

57960176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96023413-C-T

57960305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96023512-G-T

57960316-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96023523-G-C

57960383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96023633-G-A

57960383-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96023633-G-C

57960383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96023633-G-T

http://identifiers.org/hco/16/GRCh38#57960405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96023655-C-A

57960406-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96023656-T-A

57960406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96023656-T-C

57960451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96023688-G-A

57960451-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96023688-G-C

57960543-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96023764-C-G

57960548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96023769-C-T

57960596-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96023809-C-G

57960596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96023809-C-T

57960599-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96023812-C-G

57960602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96023815-G-A

57960602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96023815-G-T

57960605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96023818-G-A

57960605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96023818-G-T

http://identifiers.org/hco/16/GRCh38#57960615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96023828-C-A

57960615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96023828-C-T

http://identifiers.org/hco/16/GRCh38#57960722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96024294-C-A

57960722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96024294-C-T

57960734-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96024307-A-T

57960778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96024347-T-C

57960811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96024376-A-G

57960811-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96024376-A-T

57960884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: stop gained
orthologous variants: 96024447-G-A

http://identifiers.org/hco/16/GRCh38#57960928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96024491-C-A

57961010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96024569-T-C

57961011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96024570-G-A

57961011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96024570-G-T

57961953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96024722-A-G

57961977-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96024755-T-A

57961980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96024758-T-C

57962036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96024954-A-G

57962066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96024984-T-C

57962132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96025045-G-A

57962438-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96025314-A-T

57962442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96025318-G-T

http://identifiers.org/hco/16/GRCh38#57962544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96025413-C-A

57962639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96025497-G-A

http://identifiers.org/hco/16/GRCh38#57962829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96026099-C-A

57962938-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96026237-C-G

57962938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96026237-C-T

57962943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96026240-C-T

57962944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96026241-G-A

57962944-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96026241-G-C

57962944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96026241-G-T

57963043-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: synonymous variant
orthologous variants: 96026372-G-C

http://identifiers.org/hco/16/GRCh38#57963087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96026417-C-A

57963087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96026417-C-T

57963181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96026444-G-A

57963181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron variant
orthologous variants: 96026444-G-T

57964211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96027349-G-A

57964211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96027349-G-T

57964258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96027395-C-T

57964289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96027428-G-A

57964292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96027431-A-G

57964294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96027433-A-G

57964343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96027464-C-T

http://identifiers.org/hco/16/GRCh38#57964445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96027550-C-A

57964445-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96027550-C-G

57964445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96027550-C-T

57964452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96027557-G-T

57964500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 96027599-G-A

57964521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 96027620-C-T

57964527-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 96027626-G-C

57964541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 96027640-G-A

57964541-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 96027640-G-C

57964552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 96027650-G-T

57964562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96027660-G-A

57964600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96027690-C-T

57964603-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96027692-G-C

57964649-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96027738-T-A

57964649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96027738-T-C

57964649-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96027738-T-G

http://identifiers.org/hco/16/GRCh38#57964653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96027742-C-A

57964653-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96027742-C-G

57964653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96027742-C-T

57965862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96027752-C-T

57965863-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96027753-A-T

http://identifiers.org/hco/16/GRCh38#57965986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96027834-C-A

57965986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96027834-C-T

http://identifiers.org/hco/16/GRCh38#57966996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96030083-C-A

57966996-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96030083-C-G

57966996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96030083-C-T

57967023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96030105-G-T

57967073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96030144-G-T

57967094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96030165-G-A

57967137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 96030251-G-A

57967137-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 96030251-G-C

57967140-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 96030254-C-G

57967143-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 96030257-T-A

57967146-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 96030260-C-G

57967155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 96030272-C-T

57967158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 96030275-A-G

57967164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 96030281-C-T

57967170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 96030287-T-C

57967219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 96030389-T-C

57967219-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 96030389-T-G

57967303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 96030474-G-T

57967680-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96030727-G-T

57967705-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96030746-T-A

57967723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96030764-A-G

57967723-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96030764-A-T

57967796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96030907-T-C

57967887-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96031059-G-C

http://identifiers.org/hco/16/GRCh38#57967992-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96031155-A-C

57968100-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96031256-G-C

57968247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96031332-C-T

57968268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96031352-T-C

57968312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96031397-C-T

57968332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96031420-A-G

57968363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96031472-T-C

57969516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96031860-G-T

57969838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96032128-C-T

57970045-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96032286-C-G

57970110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96032341-G-A

57970644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96032796-C-T

57971005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96033104-A-G

http://identifiers.org/hco/16/GRCh38#57971009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96033108-C-A

http://identifiers.org/hco/16/GRCh38#57971051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96033151-C-A

57971051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96033151-C-T

http://identifiers.org/hco/16/GRCh38#57971076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96033176-C-A

57971076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 96033176-C-T

http://identifiers.org/hco/16/GRCh38#57971113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96033212-C-A

57971113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2151
most severe consequence: 5 prime UTR variant
orthologous variants: 96033212-C-T