178960174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32348645-T-C

178960186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32348658-G-A

178960187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32348659-C-T

178960192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32348664-G-A

178960244-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32348717-G-C

http://identifiers.org/hco/3/GRCh38#178960479-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#32349175-A-C

178961167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32350083-T-C

178961191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32350107-G-T

178961229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32350147-G-A

178962492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32352253-G-A

178962579-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32352334-A-T

178963124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32353537-A-G

178963333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32353744-G-T

178966673-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32371867-A-T

178966817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32372013-T-C

178967160-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32372388-T-G

178967163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32372391-T-C

178967238-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32372420-G-C

178967283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32372462-A-G

178967362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32372487-G-A

178967790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32372893-A-G

http://identifiers.org/hco/3/GRCh38#178969025-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-C

178969033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

178969265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

http://identifiers.org/hco/3/GRCh38#178971702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#32380676-C-A

178971737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32380706-G-A

178971902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32380857-T-C

http://identifiers.org/hco/3/GRCh38#178971948-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#32380924-A-C

178972196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32381339-T-C

178972212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32381355-A-G

http://identifiers.org/hco/3/GRCh38#178972230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#32381373-C-A

178972312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32381454-G-A

178972698-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32381813-T-A

178972698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32381813-T-C

178972706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32381821-A-G

179014644-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron variant
orthologous variants: 32386864-T-G

http://identifiers.org/hco/3/GRCh38#179015279-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#32387351-A-C

179015279-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron variant
orthologous variants: 32387351-A-T

179015760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron variant
orthologous variants: 32387813-T-C

179015762-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron variant
orthologous variants: 32387815-G-C

179015859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron variant
orthologous variants: 32387907-A-G

http://identifiers.org/hco/3/GRCh38#179016390-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#32388336-A-C

179017119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron variant
orthologous variants: 32388845-C-T

179017546-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32389243-C-G

http://identifiers.org/hco/3/GRCh38#179017688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#32389368-C-A

179017688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32389368-C-T

179017866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32389541-T-C

179017873-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32389548-G-C

179018047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32389721-G-A

179018047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32389721-G-T

http://identifiers.org/hco/3/GRCh38#179018070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#32389745-C-A

179018070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32389745-C-T

179018225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32389869-T-C

179018258-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32389909-T-G

179018264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32389915-G-A

179018639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32390411-A-G

179018703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32390462-T-C

http://identifiers.org/hco/3/GRCh38#179019104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#32390648-C-A

179019376-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32390809-C-G

179019376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32390809-C-T

http://identifiers.org/hco/3/GRCh38#179019772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#32391178-C-A

179019897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32391286-G-T

179020075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32391407-G-A

179020076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32391408-G-A

179020076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32391408-G-T

179020392-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32391729-A-T

179020546-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32391867-G-C

179020591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32391908-T-C

http://identifiers.org/hco/3/GRCh38#179020664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#32391979-C-A

http://identifiers.org/hco/3/GRCh38#179020830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#32392141-C-A

179020839-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32392150-C-G

179020856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32392163-G-A

http://identifiers.org/hco/3/GRCh38#179021020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#32392308-C-A

http://identifiers.org/hco/3/GRCh38#179021022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#32392310-C-A

179021022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32392310-C-T

179021305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32392570-C-T

179021634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32393048-C-T

http://identifiers.org/hco/3/GRCh38#179021706-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#32393093-A-C

179021706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32393093-A-G

179021834-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 32393197-T-A

179021860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 32393212-G-A

179021860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 32393212-G-T

179021921-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32393256-G-C

179022022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32393342-T-C

http://identifiers.org/hco/3/GRCh38#179022255-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#32393564-A-C

http://identifiers.org/hco/3/GRCh38#179022339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#32393647-C-A

179022428-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32393740-T-G

179022429-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32393741-G-C

179022479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32393819-T-C

179022607-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32393944-A-T

179022626-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32393958-T-A

179022679-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32393989-A-T

http://identifiers.org/hco/3/GRCh38#179022692-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#32394002-A-C

179022709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32394019-T-C

179022731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32394040-G-A

179022731-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32394040-G-C

179023396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32394492-G-A

179024118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32394960-A-G

179024118-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32394960-A-T

179024147-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32394989-A-T

179024153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32394995-A-G

179024180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32395009-G-A

179024180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32395009-G-T

179024181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32395010-A-G

179024226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32395054-G-A

179024271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32395098-T-C

179024271-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32395098-T-G

179024274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32395101-G-A

179024274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32395101-G-T

http://identifiers.org/hco/3/GRCh38#179024286-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#32395110-C-A

179024293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32395117-A-G

http://identifiers.org/hco/3/GRCh38#179025044-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#32395663-A-C

179025044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32395663-A-G

179025187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32395806-G-A

179025268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32396147-T-C

179025321-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32396198-A-T

179025402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32396278-G-A

179026731-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32396747-G-C

179027250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32397332-T-C

179027282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32397362-T-C

http://identifiers.org/hco/3/GRCh38#179027289-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#32397366-C-A

179027289-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32397366-C-G

179027289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32397366-C-T

http://identifiers.org/hco/3/GRCh38#179027292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#32397369-C-A

179027293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32397370-C-T

179027304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32397381-T-C

http://identifiers.org/hco/3/GRCh38#179027548-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#32397606-A-C

179027549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32397607-G-A

179027646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 32397701-G-A

179027646-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 32397701-G-C

http://identifiers.org/hco/3/GRCh38#179027711-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#32397766-A-C

179027786-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32397841-T-G

179027835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32397886-A-G

179027878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32397915-A-G

179027879-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32397916-G-T

http://identifiers.org/hco/3/GRCh38#179027904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#32397941-C-A

http://identifiers.org/hco/3/GRCh38#179027907-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#32397944-A-C

179027932-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32397969-T-A

179027938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32397975-T-C

179027962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32397995-G-A

179027962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32397995-G-T

179027963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32397996-G-A

179027963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32397996-G-T

179028106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32398118-G-A

179028629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32398582-A-G

http://identifiers.org/hco/3/GRCh38#179028662-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#32398617-A-C

179029179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32398784-G-A

179029219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32398823-T-C

179029219-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32398823-T-G

179029282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32398887-A-G

179029458-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32399060-T-A

179030778-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32399525-T-G

179030792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32399539-C-T

179030901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32399628-T-C

179031583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32400308-A-G

179031621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32400346-A-G

179033701-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32400468-T-A

179033930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32400667-A-G

179034214-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32401081-G-C

179034360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32401185-G-A

179034462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32401292-C-T

179034525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32401356-T-C

179061331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32406292-G-A

179061331-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32406292-G-C

179061569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32406524-G-A

http://identifiers.org/hco/3/GRCh38#179061647-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#32406598-A-C

http://identifiers.org/hco/3/GRCh38#179061671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#32406622-C-A

179062020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32406860-G-A

179062020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32406860-G-T

179062073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32406911-C-T

179062111-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32406953-A-T

179062394-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32407767-A-T

179062461-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32407898-C-G

179062482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32407918-C-T

http://identifiers.org/hco/3/GRCh38#179062531-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#32407961-A-C

179062560-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32408006-C-G

179062561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32408007-T-C

179063542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32409613-T-C

http://identifiers.org/hco/3/GRCh38#179063652-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#32409815-A-C

179063805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32409962-C-T

179063971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32410117-T-C

179064060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32410205-G-A

179064143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32410280-G-A

179064296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32410401-T-C

179064378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32410489-C-T

179064662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32410700-C-T

179064854-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32410815-G-C

179064854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32410815-G-T

http://identifiers.org/hco/3/GRCh38#179065240-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#32412202-A-C

179065341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32412293-A-G

179066992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32414570-A-G

179067113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32414688-G-T

179067429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32414987-A-G

179067450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32415007-T-C

179067651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32415207-T-C

179067875-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32415410-T-A

179067875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32415410-T-C

179067875-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32415410-T-G

179067928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32415453-G-A

179067934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32415459-T-C

http://identifiers.org/hco/3/GRCh38#179067947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#32415472-C-A

179067947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32415472-C-T

179067955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32415480-G-T

179068004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32415528-G-A

179068015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32415539-T-C

179068036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32415559-C-T

http://identifiers.org/hco/3/GRCh38#179068092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#32415618-C-A

179068733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32416684-T-C

179069267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32417503-T-C

http://identifiers.org/hco/3/GRCh38#179069344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#32417575-C-A

179069344-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32417575-C-G

179069344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32417575-C-T

179069366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32417597-G-A

179069476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32417893-G-A

179069476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32417893-G-T

179069512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32417933-T-C

179069866-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32418188-G-C

179070179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32418471-C-T

179070289-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32418578-T-A

179070716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32419005-G-A

179071438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32419575-C-T

179071730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32419734-G-A

179071730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32419734-G-T

179071758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32419764-G-A

179071758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32419764-G-T

http://identifiers.org/hco/3/GRCh38#179071777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#32419783-C-A

179071777-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32419783-C-G

http://identifiers.org/hco/3/GRCh38#179071934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#32419937-C-A

179071934-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 32419937-C-G

179071934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 32419937-C-T

179071941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 32419942-C-T

179071942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29983
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 32419943-G-A