160945026-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 171345692-T-A

160945026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 171345692-T-C

160945026-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 171345692-T-G

160945046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 171345712-T-C

160945059-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 171345725-T-A

http://identifiers.org/hco/1/GRCh38#160945071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#171345737-C-A

160945071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 171345737-C-T

160945076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 171345742-T-C

160945079-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 171345745-C-G

http://identifiers.org/hco/1/GRCh38#160945080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#171345746-C-A

160945080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 171345746-C-T

http://identifiers.org/hco/1/GRCh38#160945126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#171345799-C-A

160945126-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 171345799-C-G

160945126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 171345799-C-T

160945127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 171345800-G-A

160945127-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 171345800-G-C

160945127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 171345800-G-T

160945131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 171345804-A-G

http://identifiers.org/hco/1/GRCh38#160945144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#171345813-C-A

160945152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 171345821-C-T

160945161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 171345830-A-G

160945161-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 171345830-A-T

160945180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 171345849-C-T

160945182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 171345851-A-G

160945182-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 171345851-A-T

http://identifiers.org/hco/1/GRCh38#160945217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#171345886-C-A

http://identifiers.org/hco/1/GRCh38#160945219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#171345888-C-A

160945229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 171345898-C-T

160945230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 171345899-G-A

160945230-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 171345899-G-C

160945233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 171345902-G-A

160945247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained, undefined
orthologous variants: 171345916-G-A

160945248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 171345917-A-G

http://identifiers.org/hco/1/GRCh38#160945249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#171345918-C-A

160945249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 171345918-C-T

160945250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 171345919-G-A

160945256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 171345925-T-C

160945258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 171345927-C-T

160945259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 171345928-C-T

160945266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 171345935-G-A

160945284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 171345953-G-A

160945295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 171345964-G-A

160945295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 171345964-G-T

160945303-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171345972-G-C

http://identifiers.org/hco/1/GRCh38#160947916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#171356676-C-A

160947916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171356676-C-T

http://identifiers.org/hco/1/GRCh38#160947917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#171356677-C-A

160947930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 171356690-T-C

160947930-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 171356690-T-G

160947931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 171356691-G-A

160947962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 171356722-A-G

160947978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 171356738-G-T

160947998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 171356758-C-T

160948004-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 171356764-G-C

160948030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 171356790-C-T

160948036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 171356795-A-G

160948041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171356800-G-A

160948087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171356838-A-G

160948088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171356839-G-T

160948091-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171356842-T-A

http://identifiers.org/hco/1/GRCh38#160948094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#171356845-C-A

160948094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171356845-C-T

160948096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171356847-T-C

160948098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171356849-G-T

160948099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171356850-G-A

160948099-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171356850-G-T

http://identifiers.org/hco/1/GRCh38#160948105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#171356856-C-A

160948105-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171356856-C-G

160948105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171356856-C-T

160948107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171356858-A-G

160948108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171356859-G-T

160949847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 171357887-T-C

160949851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 171357891-G-T

160949854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 171357894-A-G

160949858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 171357898-G-A

http://identifiers.org/hco/1/GRCh38#160949868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#171357908-C-A

160949869-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 171357909-T-G

http://identifiers.org/hco/1/GRCh38#160949883-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#171357922-A-C

160949883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 171357922-A-G

160949886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 171357925-G-A

160949886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 171357925-G-T

160949887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 171357926-T-C

160949890-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 171357929-T-A

160949890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 171357929-T-C

160949891-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 171357930-T-A

160949891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 171357930-T-C

http://identifiers.org/hco/1/GRCh38#160949900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#171357939-C-A

http://identifiers.org/hco/1/GRCh38#160949918-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#171357956-C-A

160949918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 171357956-C-T

160949920-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 171357958-A-T

160949924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171357962-A-G

160949926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171357964-G-A

160949926-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171357964-G-T

160949929-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171357967-T-A

160949952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171357984-T-C

160949955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171357987-A-G

http://identifiers.org/hco/1/GRCh38#160949958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#171357991-C-A

http://identifiers.org/hco/1/GRCh38#160949988-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#171358019-C-A

160950011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171358046-A-G

160950039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 171358055-C-T

160950041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171358057-C-T

160950054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 171358070-T-C

160950071-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 171358087-T-A

160950112-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 171358128-T-A

160950119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 171358135-G-A

160950141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 171358157-C-T

160950144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 171358160-G-A

160950147-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 171358163-C-G

160950149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 171358165-G-A

160950158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 171358174-T-C

160950180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171358193-G-A

160950180-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171358193-G-C

160950181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171358194-A-G

160950183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171358196-G-A

160950183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171358196-G-T

http://identifiers.org/hco/1/GRCh38#160950186-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#171358200-A-C

160950188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171358202-G-A

160950211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171358239-C-T

160950216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171358244-A-G

160950225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171358253-G-A

160950225-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171358253-G-C

160950225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171358253-G-T

160950234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171358262-G-A

160950234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171358262-G-T

160950235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171358263-G-A

160950235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171358263-G-T

http://identifiers.org/hco/1/GRCh38#160950240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#171358271-C-A

http://identifiers.org/hco/1/GRCh38#160950247-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#171358278-A-C

160950250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171358281-G-A

160950250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171358281-G-T

http://identifiers.org/hco/1/GRCh38#160950269-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#171358300-C-A

160950269-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171358300-C-G

160950269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171358300-C-T

160950272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171358303-C-T

160950281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171358312-G-A

160950281-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171358312-G-T

160950311-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171358346-A-T

160950315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171358353-G-A

160950315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171358353-G-T

160950382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171358452-G-A

160950384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171358454-C-T

160950428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171358491-A-G

160950428-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171358491-A-T

160950429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171358492-G-A

160950429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171358492-G-T

160950433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171358496-G-A

160950433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171358496-G-T

http://identifiers.org/hco/1/GRCh38#160950443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#171358506-C-A

160950443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171358506-C-T

160950447-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171358510-C-G

160950451-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171358514-T-G

160950472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171358522-A-G

160950472-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171358522-A-T

160950478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171358528-G-T

160950483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171358532-G-A

http://identifiers.org/hco/1/GRCh38#160950484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#171358533-C-A

160950484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171358533-C-T

160950485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171358534-C-T

160950486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171358535-C-T

http://identifiers.org/hco/1/GRCh38#160950488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#171358537-C-A

160950488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171358537-C-T

http://identifiers.org/hco/1/GRCh38#160950491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#171358540-C-A

160950491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171358540-C-T

160950505-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171358554-A-T

160950511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171358560-G-T

http://identifiers.org/hco/1/GRCh38#160950516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#171358565-C-A

160950516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171358565-C-T

160950517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171358566-C-T

160950521-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171358570-G-C

160950527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171358576-G-A

http://identifiers.org/hco/1/GRCh38#160950541-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#171358590-A-C

160950544-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 171358593-C-G

160950562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 171358611-G-A

http://identifiers.org/hco/1/GRCh38#160950571-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#171358620-A-C

160950577-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 171358626-T-A

160950582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 171358631-G-A

http://identifiers.org/hco/1/GRCh38#160950584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#171358633-C-A

160950584-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 171358633-C-G

160950589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 171358638-G-A

160950589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 171358638-G-T

160950609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 171358658-G-A

160950628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 171358677-G-A

160950638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 171358687-T-C

http://identifiers.org/hco/1/GRCh38#160950664-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#171358713-A-C

160950664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 171358713-A-G

160950664-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 171358713-A-T

160950691-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 171358740-G-C

160950697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 171358746-G-A

160950697-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 171358746-G-C

160950729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 171358778-C-T

http://identifiers.org/hco/1/GRCh38#160950734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#171358783-C-A

160950743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 171358792-G-A

160950748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 171358797-G-T

160950760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 171358809-G-A

160950766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 171358815-A-G

160950771-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 171358820-C-G

http://identifiers.org/hco/1/GRCh38#160950773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#171358822-C-A

160950773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 171358822-C-T

160950779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 171358828-C-T

160950781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 171358830-G-A

160950787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 171358837-G-A

160950792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 171358842-G-A

160950792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 171358842-G-T

160950799-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 171358849-G-C

160950799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 171358849-G-T

160950825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 171358861-A-G

http://identifiers.org/hco/1/GRCh38#160950827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#171358863-C-A

160950827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 171358863-C-T

160950828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 171358864-C-T

160950831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 171358867-G-A

160950831-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 171358867-G-C

160950831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 171358867-G-T

http://identifiers.org/hco/1/GRCh38#160950832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#171358868-C-A

160950832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 171358868-C-T

http://identifiers.org/hco/1/GRCh38#160950842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#171358878-C-A

160950842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 171358878-C-T

http://identifiers.org/hco/1/GRCh38#160950843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#171358880-C-A

160950843-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 171358880-C-G

160950843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 171358880-C-T

160950847-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 171358884-C-G

160950851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 171358890-G-T

http://identifiers.org/hco/1/GRCh38#160950878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#171358917-C-A

160950879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 171358918-C-T

http://identifiers.org/hco/1/GRCh38#160950883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#171358922-C-A

160950883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 171358922-C-T

http://identifiers.org/hco/1/GRCh38#160950886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#171358925-C-A

160950886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 171358925-C-T

160950889-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 171358928-T-G

160950890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 171358929-G-T

160950896-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 171358934-A-T

160950898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 171358936-G-T

160950926-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 171358964-C-G

160950927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 171358965-T-C

160950958-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 171358993-C-G

160950958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 171358993-C-T

160950963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 171358998-C-T

160950979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 171359014-A-G

160950992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 171359022-G-A

160950994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 171359024-C-T

160951012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 171359042-C-T

160951036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 171359067-C-T

160951065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 171359096-G-A

160951157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 171359188-A-G

http://identifiers.org/hco/1/GRCh38#160951160-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#171359191-C-A

160951160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 171359191-C-T

160951170-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 171359201-T-G

http://identifiers.org/hco/1/GRCh38#160951175-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#171359206-A-C

160951175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 171359206-A-G

160951176-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 171359207-C-G

160951176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 171359207-C-T

160951177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 171359208-G-A

160951177-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 171359208-G-C

160951180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 171359211-T-C

160951184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 171359215-A-G

160951190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 171359221-G-A

160951229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 171359260-A-G

160951267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 171359298-T-C

160951271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 171359302-G-A

http://identifiers.org/hco/1/GRCh38#160951272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#171359303-C-A

160951272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 171359303-C-T

160951276-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 171359307-G-C

160951286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 171359317-G-A

160951286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 171359317-G-T

160951300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 171359331-G-A

160951300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 171359331-G-T

http://identifiers.org/hco/1/GRCh38#160951315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#171359346-C-A

160951315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 171359346-C-T

160951316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 171359347-T-C

http://identifiers.org/hco/1/GRCh38#160951332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#171359363-C-A

160951332-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 171359363-C-G

160951332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 171359363-C-T

160951334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 171359365-G-T

160951335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 171359366-G-T

160951336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 171359367-G-A

160951336-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 171359367-G-T

http://identifiers.org/hco/1/GRCh38#160951342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#171359373-C-A

160951347-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 171359378-C-G

160951347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 171359378-C-T

160951351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 171359382-G-A

160951351-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 171359382-G-C

160951351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 171359382-G-T

160951353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 171359384-G-T

160951356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 171359387-T-C

160951361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 171359392-A-G

http://identifiers.org/hco/1/GRCh38#160951364-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#171359395-C-A

160951366-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 171359397-C-G

160951366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 171359397-C-T

http://identifiers.org/hco/1/GRCh38#160952622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: missense_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#171360936-C-A

160952622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 171360936-C-T

160952631-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: missense variant
orthologous variants: 171360945-T-G

160952637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: missense variant
orthologous variants: 171360951-C-T

160952642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: synonymous variant
orthologous variants: 171360956-C-T

160952654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: synonymous variant
orthologous variants: 171360968-G-A

160952673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: missense variant
orthologous variants: 171360987-G-A

160952673-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: missense variant
orthologous variants: 171360987-G-C

160952678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: synonymous variant
orthologous variants: 171360992-G-A

160952678-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: synonymous variant
orthologous variants: 171360992-G-C

160954380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 171362315-C-T

http://identifiers.org/hco/1/GRCh38#160954397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#171362332-C-A

160954397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: synonymous_variant, undefined
orthologous variants: 171362332-C-T

160954404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: missense_variant, undefined
orthologous variants: 171362339-G-A

160954404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: missense_variant, undefined
orthologous variants: 171362339-G-T

160954406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: synonymous_variant, undefined
orthologous variants: 171362341-G-A

160954406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: synonymous_variant, undefined
orthologous variants: 171362341-G-T

http://identifiers.org/hco/1/GRCh38#160954409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#171362344-C-A

160954409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: synonymous_variant, undefined
orthologous variants: 171362344-C-T

http://identifiers.org/hco/1/GRCh38#160954411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: missense_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#171362346-C-A

160954411-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: missense_variant, undefined
orthologous variants: 171362346-C-G

160954411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: missense_variant, undefined
orthologous variants: 171362346-C-T

160954430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: synonymous_variant, undefined
orthologous variants: 171362365-G-A

160954430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: stop_gained, undefined
orthologous variants: 171362365-G-T

160954432-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: missense_variant, undefined
orthologous variants: 171362367-A-T

160954433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: synonymous variant
orthologous variants: 171362368-G-A

160954433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: synonymous variant
orthologous variants: 171362368-G-T

http://identifiers.org/hco/1/GRCh38#160954449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: missense_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#171362384-C-A

160954449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: missense_variant, splice_region_variant, undefined
orthologous variants: 171362384-C-T

160954453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 171362388-A-G

160954455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 171362390-G-A

160954455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 171362390-G-T

160954456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 171362391-G-A

160954456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 171362391-G-T

160954461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, undefined
orthologous variants: 171362396-A-G

160954474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, undefined
orthologous variants: 171362406-G-A

160954474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, undefined
orthologous variants: 171362406-G-T

160954525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, undefined
orthologous variants: 171362456-T-C

160954525-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20599
most severe consequence: intron_variant, undefined
orthologous variants: 171362456-T-G