http://identifiers.org/hco/4/GRCh38#145680160-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#79975124-C-A

http://identifiers.org/hco/4/GRCh38#145680183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#79975101-C-A

145680183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: 5 prime UTR variant
orthologous variants: 79975101-C-T

http://identifiers.org/hco/4/GRCh38#145680192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#79975092-C-A

145680210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: missense variant
orthologous variants: 79975073-C-T

145680273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: missense variant
orthologous variants: 79975010-G-T

http://identifiers.org/hco/4/GRCh38#145680417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#79974866-C-A

145680735-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: 79974630-C-G

http://identifiers.org/hco/4/GRCh38#145681499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#79973348-C-A

145682246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: 79973078-A-G

145682308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: 79973025-T-C

145682437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: 79972898-A-G

145692371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: 79956982-T-C

145692669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: 79956675-G-A

145696500-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: 79956079-T-G

145696507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: 79956072-G-A

145696508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: 79956071-A-G

145696508-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: 79956071-A-T

145696544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: 79956035-A-G

145696650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: 79955929-A-G

145715099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: 79955149-T-C

145715160-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: 79955098-G-T

145715420-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: 79954878-C-G

http://identifiers.org/hco/4/GRCh38#145715875-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#79954484-A-C

145716022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: 79954362-C-T

145716480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, undefined
orthologous variants: 79953978-G-T

145716489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: 79953969-G-A

145716489-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: 79953969-G-C

145716932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: 79953546-G-T

145716934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: 79953544-A-G

145717060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: 79953218-T-C

145717182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: 79953104-G-A

145717182-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: 79953104-G-C

145720813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: 79949569-A-G

145720840-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: 79949543-C-G

145720840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: 79949543-C-T

145720923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: 79949456-A-G

145720939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: 79949435-C-T

145721363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: 79949305-G-A

145721396-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: 79949272-T-A

145721396-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: 79949272-T-G

145721920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: 79948753-A-G

145722033-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: 79948650-T-G

145722320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: 79948288-G-A

145722654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: 79948065-A-G

145723270-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: 79947955-T-A

145723449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: 79947767-T-C

145723495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: 79947756-C-T

145723496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: 79947755-C-T

145723524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: 79947727-C-T

http://identifiers.org/hco/4/GRCh38#145723708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#79947568-C-A

145726930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 79946913-C-T

145726932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, missense_variant
orthologous variants: 79946911-G-A

145727014-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: 79946828-A-T

145727127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: 79946718-A-G

http://identifiers.org/hco/4/GRCh38#145727182-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#79946669-A-C

145729054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: 79941637-A-G

http://identifiers.org/hco/4/GRCh38#145729158-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#79941603-C-A

145729158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: 79941603-C-T

145729757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: 79941275-G-A

145729757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: 79941275-G-T

145729759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: 79941273-A-G

145729759-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: 79941273-A-T

145729760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: 79941272-G-A

145729760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: 79941272-G-T

145729874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: 79940202-G-A

145729962-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: missense variant
orthologous variants: 79940108-G-C

145730044-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: 79940057-G-C

145730044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: 79940057-G-T

http://identifiers.org/hco/4/GRCh38#145730147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#79939974-C-A

145730147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: 79939974-C-T

145730260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: 79939882-C-T

145730325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: 79939810-T-C

145730354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: 79939790-T-C

145730614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: 79938946-G-T

145730867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: 79938692-A-G

145731590-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: 79938095-T-G

http://identifiers.org/hco/4/GRCh38#145731611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#79938084-C-A

145731963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: 79937872-C-T

145732283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: 79937567-A-G

145732306-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: 79937539-A-T

145732348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: 79937490-T-C

http://identifiers.org/hco/4/GRCh38#145732382-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#79937456-A-C

145732382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: 79937456-A-G

145732382-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron variant
orthologous variants: 79937456-A-T

145732752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79937089-G-A

145732752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79937089-G-T

145732833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79937016-A-G

145732873-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79936976-C-G

145733386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79936765-G-A

145733535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79936693-C-T

145733834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79936426-T-C

145734360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79935910-G-T

145734497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79935827-G-T

145734536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79935785-A-G

145734970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79935391-G-A

145734970-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79935391-G-C

145735149-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79935055-A-T

145735625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79934658-G-A

145736244-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79934065-G-C

145736253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79934056-C-T

145736949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79933420-G-A

145736949-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79933420-G-C

145736991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79933347-C-T

145737042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79933295-C-T

145737986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79932383-A-G

145738011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79932355-G-A

145738011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79932355-G-T

145739349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79931415-A-G

145740104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79930646-C-T

145740185-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79930593-C-G

145740185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79930593-C-T

145740303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79929098-G-A

145740333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79929065-A-G

145740556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79928770-C-T

145740613-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79928713-C-G

145740752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79928586-G-A

145741399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79927996-A-G

145741490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79927903-C-T

145741655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79927745-T-C

145744201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79925779-G-A

145744201-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79925779-G-C

145744201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79925779-G-T

145744521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79925507-C-T

145753336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79925209-A-G

145753427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79925119-C-T

145753445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79925102-A-G

145753662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79924901-T-C

http://identifiers.org/hco/4/GRCh38#145753884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#79924660-C-A

145753884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79924660-C-T

http://identifiers.org/hco/4/GRCh38#145754061-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#79924437-C-A

145754061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79924437-C-T

http://identifiers.org/hco/4/GRCh38#145754130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#79924369-C-A

145754447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79923282-G-A

145754447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79923282-G-T

http://identifiers.org/hco/4/GRCh38#145754523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#79923213-C-A

145755282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79922547-T-C

145755293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79922527-G-A

145755358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79922465-G-T

145755485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79922373-A-G

145755657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79922213-C-T

145755761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79922119-C-T

145756010-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79921888-C-G

145756010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79921888-C-T

145756132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79921780-G-A

145756136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79921776-T-C

145756322-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79921613-A-T

145756330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79921607-T-C

145756425-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79921547-T-A

145756504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79921486-C-T

145756654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79921325-G-A

145756691-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79921296-T-G

145756719-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79921267-C-G

145756729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79921257-T-C

145757010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79920994-A-G

145757117-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79920899-C-G

http://identifiers.org/hco/4/GRCh38#145757575-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#79920445-A-C

145758022-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79919962-C-G

145758601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79919363-A-G

145758736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79919228-T-C

http://identifiers.org/hco/4/GRCh38#145758830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#79919114-C-A

145758846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79919098-G-A

145758846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79919098-G-T

http://identifiers.org/hco/4/GRCh38#145758870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#79919075-C-A

145758870-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79919075-C-G

http://identifiers.org/hco/4/GRCh38#145759223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#79918753-C-A

145759915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79918040-G-A

145760246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79917702-G-T

145760342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79917541-A-G

145760388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79917494-G-T

145760427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79917455-G-A

145760427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79917455-G-T

145760459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79917424-T-C

145760486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79917397-G-T

145760504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79917381-G-T

145760641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79917249-G-T

145760667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79917224-T-C

145760667-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79917224-T-G

145761052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 79916840-C-T

145761629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79916260-A-G

http://identifiers.org/hco/4/GRCh38#145761680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#79916209-C-A

http://identifiers.org/hco/4/GRCh38#145761726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#79916172-C-A

145761726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79916172-C-T

http://identifiers.org/hco/4/GRCh38#145761773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#79916133-C-A

145761773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79916133-C-T

145762343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79915526-G-T

http://identifiers.org/hco/4/GRCh38#145763356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#79914541-C-A

145763510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79914391-G-A

http://identifiers.org/hco/4/GRCh38#145763806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#79914134-C-A

145763806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79914134-C-T

http://identifiers.org/hco/4/GRCh38#145763829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#79914110-C-A

145763840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79914105-A-G

145763887-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79914052-G-C

http://identifiers.org/hco/4/GRCh38#145764537-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#79913423-A-C

145764568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79913389-G-A

145764568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79913389-G-T

145764640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79913313-T-C

145764667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79913288-G-A

145764667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79913288-G-T

http://identifiers.org/hco/4/GRCh38#145764709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#79913255-C-A

145764709-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79913255-C-G

145764709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79913255-C-T

145764726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79913238-G-A

145764726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79913238-G-T

http://identifiers.org/hco/4/GRCh38#145764734-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#79913230-A-C

http://identifiers.org/hco/4/GRCh38#145764768-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#79913199-A-C

145764861-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79913107-A-T

http://identifiers.org/hco/4/GRCh38#145764865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#79913103-C-A

http://identifiers.org/hco/4/GRCh38#145764875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#79913093-C-A

145764875-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79913093-C-G

145764875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79913093-C-T

145764906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79913061-T-C

145764921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79913048-G-A

145764921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79913048-G-T

145764933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79913035-G-A

145765219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79912723-G-A

145765219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79912723-G-T

http://identifiers.org/hco/4/GRCh38#145765262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#79912658-C-A

145765262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79912658-C-T

http://identifiers.org/hco/4/GRCh38#145765273-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#79912647-C-A

145765273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79912647-C-T

145765288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79912632-A-G

145765327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79912595-A-G

145765435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79912500-A-G

145765435-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79912500-A-T

http://identifiers.org/hco/4/GRCh38#145765475-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#79912483-A-C

145765495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79912463-G-A

145765708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79912255-T-C

http://identifiers.org/hco/4/GRCh38#145765840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#79912142-C-A

http://identifiers.org/hco/4/GRCh38#145765856-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#79912130-A-C

145766344-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79911628-T-A

145766703-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79911309-C-G

145766703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79911309-C-T

145766816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79911201-A-G

145766892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79911118-T-C

145773073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79908025-G-T

145773292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79907805-T-C

145774418-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79906911-G-T

145774435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79906894-G-A

145774435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79906894-G-T

http://identifiers.org/hco/4/GRCh38#145774450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#79906879-C-A

http://identifiers.org/hco/4/GRCh38#145774452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#79906877-C-A

145774459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79906870-G-A

145774459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79906870-G-T

http://identifiers.org/hco/4/GRCh38#145774747-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#79906609-A-C

145774747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79906609-A-G

145774758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79906598-A-G

145774806-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79906555-T-A

145775223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79906176-C-T

145775420-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79906056-T-G

145775678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37264
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79905850-G-A