129647870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 3 prime UTR variant
orthologous variants: 115995661-T-C

129647936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 3 prime UTR variant
orthologous variants: 115995726-G-A

129647936-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 3 prime UTR variant
orthologous variants: 115995726-G-C

129648011-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 3 prime UTR variant
orthologous variants: 115995804-C-G

129648011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 3 prime UTR variant
orthologous variants: 115995804-C-T

http://identifiers.org/hco/3/GRCh38#129648187-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#115995978-A-C

129648187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 3 prime UTR variant
orthologous variants: 115995978-A-G

129648354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 3 prime UTR variant
orthologous variants: 115996134-C-T

129648530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 3 prime UTR variant
orthologous variants: 115996285-A-G

129648680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 3 prime UTR variant
orthologous variants: 115996423-G-A

129648863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 3 prime UTR variant
orthologous variants: 115996612-G-A

129648863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 3 prime UTR variant
orthologous variants: 115996612-G-T

http://identifiers.org/hco/3/GRCh38#129649026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#115996775-C-A

129649170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 3 prime UTR variant
orthologous variants: 115996869-T-C

129649349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 3 prime UTR variant
orthologous variants: 115997049-A-G

129649390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 3 prime UTR variant
orthologous variants: 115997085-T-C

129649662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 3 prime UTR variant
orthologous variants: 115997293-A-G

129649816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 3 prime UTR variant
orthologous variants: 115997440-A-G

129649857-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 3 prime UTR variant
orthologous variants: 115997472-T-G

http://identifiers.org/hco/3/GRCh38#129649884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#115997499-C-A

129649884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 3 prime UTR variant
orthologous variants: 115997499-C-T

http://identifiers.org/hco/3/GRCh38#129650353-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#115997961-C-A

http://identifiers.org/hco/3/GRCh38#129650531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#115998104-C-A

129650531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 3 prime UTR variant
orthologous variants: 115998104-C-T

129650535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 115998108-T-C

129650643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 3 prime UTR variant
orthologous variants: 115998255-T-C

http://identifiers.org/hco/3/GRCh38#129650716-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#115998328-C-A

129650716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 3 prime UTR variant
orthologous variants: 115998328-C-T

129650717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 3 prime UTR variant
orthologous variants: 115998329-G-A

http://identifiers.org/hco/3/GRCh38#129650772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#115998397-C-A

129650772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 3 prime UTR variant
orthologous variants: 115998397-C-T

129650780-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 3 prime UTR variant
orthologous variants: 115998405-G-C

129650780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 3 prime UTR variant
orthologous variants: 115998405-G-T

129650839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 3 prime UTR variant
orthologous variants: 115998461-G-T

http://identifiers.org/hco/3/GRCh38#129650847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#115998469-C-A

129650870-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 3 prime UTR variant
orthologous variants: 115998491-T-A

129650900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 3 prime UTR variant
orthologous variants: 115998521-G-T

129650930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 3 prime UTR variant
orthologous variants: 115998550-C-T

129651041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 3 prime UTR variant
orthologous variants: 115998642-A-G

129651057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 3 prime UTR variant
orthologous variants: 115998658-G-T

http://identifiers.org/hco/3/GRCh38#129651116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#115998695-C-A

129651116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 3 prime UTR variant
orthologous variants: 115998695-C-T

http://identifiers.org/hco/3/GRCh38#129651171-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#115998749-A-C

129651171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 3 prime UTR variant
orthologous variants: 115998749-A-G

129651178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 3 prime UTR variant
orthologous variants: 115998756-T-C

http://identifiers.org/hco/3/GRCh38#129651195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#115998773-C-A

129651254-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 3 prime UTR variant
orthologous variants: 115998827-G-C

129651254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 3 prime UTR variant
orthologous variants: 115998827-G-T

129651317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 3 prime UTR variant
orthologous variants: 115998890-T-C

129651317-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 3 prime UTR variant
orthologous variants: 115998890-T-G

http://identifiers.org/hco/3/GRCh38#129651333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#115998906-C-A

129651362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 3 prime UTR variant
orthologous variants: 115998935-A-G

129651362-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 3 prime UTR variant
orthologous variants: 115998935-A-T

129651409-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 3 prime UTR variant
orthologous variants: 115998976-G-C

129651409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 3 prime UTR variant
orthologous variants: 115998976-G-T

129651439-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 115999006-G-T

129651444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 115999011-C-T

129651450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 3 prime UTR variant
orthologous variants: 115999017-A-G

129651484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: synonymous variant
orthologous variants: 115999051-T-C

129651504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: missense variant
orthologous variants: 115999071-G-A

129651504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: synonymous variant
orthologous variants: 115999071-G-T

129651511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: synonymous variant
orthologous variants: 115999078-A-G

129651580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: synonymous_variant, undefined
orthologous variants: 115999147-C-T

129651581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: missense_variant, undefined
orthologous variants: 115999148-G-A

129651589-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: synonymous variant
orthologous variants: 115999156-G-C

129651591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: missense variant
orthologous variants: 115999158-G-A

129651591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: missense variant
orthologous variants: 115999158-G-T

129651603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: missense_variant, undefined
orthologous variants: 115999170-G-T

129651628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: synonymous variant
orthologous variants: 115999195-G-A

129651696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: missense_variant, undefined
orthologous variants: 115999263-G-A

129651696-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: missense_variant, undefined
orthologous variants: 115999263-G-C

129651702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: missense_variant, undefined
orthologous variants: 115999269-T-C

129651703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: synonymous_variant, undefined
orthologous variants: 115999270-G-A

129651771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: missense_variant, undefined
orthologous variants: 115999338-G-A

http://identifiers.org/hco/3/GRCh38#129651855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#115999416-C-A

129651891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron_variant, undefined
orthologous variants: 115999447-T-C

129651897-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron_variant, undefined
orthologous variants: 115999453-T-A

129651897-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron_variant, undefined
orthologous variants: 115999453-T-G

129652001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron_variant, undefined
orthologous variants: 115999546-C-T

129652045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron_variant, undefined
orthologous variants: 115999605-T-C

129654671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116001529-T-C

129654785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116001632-C-T

http://identifiers.org/hco/3/GRCh38#129654886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116001710-C-A

129655028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 116001823-T-C

http://identifiers.org/hco/3/GRCh38#129655177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116001965-C-A

129655177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116001965-C-T

129655283-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116002067-G-C

http://identifiers.org/hco/3/GRCh38#129655288-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116002072-A-C

http://identifiers.org/hco/3/GRCh38#129656699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#116007064-C-A

129657483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116008246-T-C

http://identifiers.org/hco/3/GRCh38#129663477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#116012590-C-A

129663477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron_variant, undefined
orthologous variants: 116012590-C-T

129663937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116013193-G-A

129664435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116014426-C-T

129664981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116014882-G-T

129665239-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron_variant, undefined
orthologous variants: 116015240-T-A

129665419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116015472-T-C

129665585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116015608-T-C

129665677-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116015706-T-A

129665955-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116016205-C-G

129665955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116016205-C-T

129666179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116016463-A-G

129667698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116017132-G-T

http://identifiers.org/hco/3/GRCh38#129667857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116017277-C-A

129669349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116019007-T-C

129669349-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116019007-T-G

129669730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116019173-T-C

129670129-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116019611-T-A

129670352-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: missense variant
orthologous variants: 116019854-T-A

129670368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: synonymous variant
orthologous variants: 116019870-A-G

http://identifiers.org/hco/3/GRCh38#129670374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116019876-C-A

129670374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: synonymous variant
orthologous variants: 116019876-C-T

129670384-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: missense variant
orthologous variants: 116019886-T-A

129670384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: missense variant
orthologous variants: 116019886-T-C

129670397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: missense variant
orthologous variants: 116019899-T-C

129670401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: synonymous variant
orthologous variants: 116019903-A-G

129670410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: synonymous variant
orthologous variants: 116019912-C-T

129670417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: missense variant
orthologous variants: 116019919-C-T

129670433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: missense variant
orthologous variants: 116019935-G-A

129670434-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: missense variant
orthologous variants: 116019936-G-C

129670434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: synonymous variant
orthologous variants: 116019936-G-T

129670445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: missense variant
orthologous variants: 116019947-T-C

129670451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: missense variant
orthologous variants: 116019953-G-T

129670452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: synonymous variant
orthologous variants: 116019954-T-C

129670455-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: synonymous variant
orthologous variants: 116019957-T-A

129670455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: synonymous variant
orthologous variants: 116019957-T-C

129670485-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: synonymous variant
orthologous variants: 116019987-C-G

129670494-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: synonymous variant
orthologous variants: 116019996-T-G

129670504-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: missense variant
orthologous variants: 116020006-C-G

129670532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: missense variant
orthologous variants: 116020034-T-C

129670539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: synonymous variant
orthologous variants: 116020041-G-A

129670551-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: synonymous variant
orthologous variants: 116020053-T-A

129670626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: synonymous variant
orthologous variants: 116020128-C-T

http://identifiers.org/hco/3/GRCh38#129670631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116020133-C-A

129670631-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: missense variant
orthologous variants: 116020133-C-G

129670650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: synonymous variant
orthologous variants: 116020152-T-C

129670748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: missense variant
orthologous variants: 116020250-C-T

129670751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: missense variant
orthologous variants: 116020253-C-T

129670884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 116020386-C-T

129670894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 116020396-C-T

129670921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 116020423-C-T

129670953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 116020455-T-C

129670986-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 116020488-G-C

http://identifiers.org/hco/3/GRCh38#129671014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116020516-C-A

129671014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 116020516-C-T

129671035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 116020537-G-A

129671073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 116020575-G-A

129671078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 116020580-G-A

129671087-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 116020589-G-C

129671147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 116020649-C-T

129671159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5_prime_UTR_variant, stop_gained
orthologous variants: 116020661-G-A

129671159-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 116020661-G-C

http://identifiers.org/hco/3/GRCh38#129671219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116020721-C-A

129671223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 116020725-A-G

http://identifiers.org/hco/3/GRCh38#129671242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116020744-C-A

129671242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 116020744-C-T

129671258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 116020760-G-A

http://identifiers.org/hco/3/GRCh38#129671388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116020880-C-A

129671388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116020880-C-T

129671752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116021148-C-T

129672726-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116021914-G-C

129673401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116023034-T-C

129684201-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116028880-C-G

129684201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116028880-C-T

129684375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116029038-T-C

129684501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116030195-T-C

http://identifiers.org/hco/3/GRCh38#129684627-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116030331-C-A

129684809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116030532-G-A

129685533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116031014-G-A

129688187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 116033497-T-C

129688209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 116033519-G-A

129688209-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 116033519-G-C

129688209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 116033519-G-T

129688228-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 116033538-C-G

129688228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 116033538-C-T

129688233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 116033543-T-C

129688271-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 116033580-A-T

129688315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 116033627-C-T

129688334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 116033646-G-A

129688336-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 116033648-A-T

129688337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 116033649-G-A

129688341-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 116033653-T-A

129688411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 116033701-T-C

129688417-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 116033707-T-A

129688417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 116033707-T-C

129688465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 116033758-G-A

129688465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 116033758-G-T

129688506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 116033797-A-G

129688532-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 116033823-T-A

129688532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 116033823-T-C

http://identifiers.org/hco/3/GRCh38#129688548-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116033838-C-A

129688548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 116033838-C-T

129688584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 116033879-G-T

129688666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 116033948-A-G

http://identifiers.org/hco/3/GRCh38#129688687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116033968-C-A

129688687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 116033968-C-T

129688857-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116034217-T-A

129689045-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116034374-G-C

http://identifiers.org/hco/3/GRCh38#129689087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116034415-C-A

129690156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116035019-C-T

129690679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116035734-G-A

129690756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116035776-C-T

129703171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116044234-T-C

129703254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116044337-G-A

http://identifiers.org/hco/3/GRCh38#129703396-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116044480-A-C

http://identifiers.org/hco/3/GRCh38#129703519-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116044599-A-C

129703558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116044634-G-A

129710620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116045550-A-G

129713018-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116046643-T-A

129713018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116046643-T-C

http://identifiers.org/hco/3/GRCh38#129713098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116046742-C-A

129713098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116046742-C-T

129713516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116047188-C-T

129723180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116049286-T-C

129723342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116049436-G-T

129723426-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116049476-A-T

129723632-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116049683-A-T

129723659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116049711-A-G

129724189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116050193-T-C

129734707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116055068-A-G

129734707-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116055068-A-T

129739532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116057148-T-C

129740137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116057748-C-T

129740276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116057880-C-T

129740301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116057905-C-T

129740522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116058157-C-T

129740562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116058189-G-A

129743979-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116061251-C-G

129744155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116061633-T-C

129744807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116061985-A-G

129744853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116062029-C-T

129744984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116062128-G-A

129744984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116062128-G-T

129745374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116062439-T-C

129745374-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116062439-T-G

129745579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116062632-A-G

129746491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116062733-A-G

http://identifiers.org/hco/3/GRCh38#129746925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116063318-C-A

129746925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116063318-C-T

129747209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116063552-A-G

http://identifiers.org/hco/3/GRCh38#129747385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: -C-A

129750534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116064608-C-T

http://identifiers.org/hco/3/GRCh38#129752382-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116065192-A-C

129764676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116066872-C-T

129768371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116069428-A-G

129771908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116071978-G-A

129772018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116072072-C-T

http://identifiers.org/hco/3/GRCh38#129777940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116078519-C-A

129777940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116078519-C-T

129787876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116079014-T-C

129788266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116079628-G-A

129788767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116079807-C-T

129788928-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116079961-C-G

129788949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116079983-T-C

129789236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116080291-C-T

129789375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116081082-G-A

129789375-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116081082-G-C

129789393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116081104-C-T

129789803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116081219-T-C

129791614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116082004-C-T

129791843-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116082339-G-C

129793034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116083071-C-T

129793247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116083257-C-T

129793279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116083268-C-T

129793325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116083319-T-C

129793360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116083343-G-A

http://identifiers.org/hco/3/GRCh38#129793406-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116083387-A-C

129793750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116083701-C-T

129793945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116083908-G-A

129794259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116084214-A-G

http://identifiers.org/hco/3/GRCh38#129794399-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116084348-A-C

129794780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116084679-A-G

http://identifiers.org/hco/3/GRCh38#129794948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116084794-C-A

129794948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116084794-C-T

129795371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116085152-T-C

http://identifiers.org/hco/3/GRCh38#129804571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116092862-C-A

129804596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116092885-T-C

129804609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116092898-T-C

129804780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116093008-G-A

129804901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116093332-G-A

http://identifiers.org/hco/3/GRCh38#129805130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116093598-C-A

129810389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116096791-T-C

129810763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116097083-A-G

129821609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116103178-G-A

129821609-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: 116103178-G-C

http://identifiers.org/hco/3/GRCh38#129823388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116103579-C-A

http://identifiers.org/hco/3/GRCh38#129823546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116103761-C-A

http://identifiers.org/hco/3/GRCh38#129825392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116106545-C-A

129827830-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116110755-T-A

129827830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116110755-T-C

129828532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116111456-A-G

http://identifiers.org/hco/3/GRCh38#129828533-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116111457-A-C

http://identifiers.org/hco/3/GRCh38#129828537-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116111461-A-C

129830547-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116113723-G-C

129830791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116113964-C-T

129830829-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116114000-C-G

129831689-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116114486-T-A

129832430-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116114837-G-C

129833250-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116115738-G-C

129835788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116117413-G-A

129835788-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116117413-G-C

129835989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116117593-T-C

129845357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116119838-C-T

129845578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116120011-A-G

129845798-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116120798-T-G

129849800-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116123810-A-T

129850164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116124066-G-A

129850219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116124119-G-A

129851126-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116124462-A-T

129851403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116124764-T-C

129856547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116130777-A-G

129856629-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116130852-A-T

129856772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116130986-T-C

129859240-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116133606-T-A

129865095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116142669-G-A

129865516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116143936-A-G

129865639-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116144053-A-T

129867011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 116144932-T-C

129867054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116144960-C-T

129867103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 116145010-G-A

http://identifiers.org/hco/3/GRCh38#129868151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116153064-C-A

129868151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116153064-C-T

129868167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116153080-T-C

129868978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116153606-T-C

129869034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116153661-T-C

129869151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116154126-A-G

129869255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116154222-G-A

http://identifiers.org/hco/3/GRCh38#129869332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116154296-C-A

http://identifiers.org/hco/3/GRCh38#129869631-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116154590-A-C

129872335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116161475-A-G

129872554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116161633-A-G

129874165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116162438-T-C

129875610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116163787-T-C

129876434-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116164126-T-A

129889076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116165254-A-G

129889165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116165389-C-T

129889201-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116165426-T-A

129889220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116165449-T-C

http://identifiers.org/hco/3/GRCh38#129889361-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116165556-A-C

129889745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116165929-G-A

129889921-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116166278-T-A

129890218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116166471-T-C

129890290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116166535-T-C

http://identifiers.org/hco/3/GRCh38#129890522-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116166720-A-C

129891020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116167758-T-C

129891020-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116167758-T-G

129891976-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116168586-G-C

129892110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116168722-T-C

http://identifiers.org/hco/3/GRCh38#129892622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116169484-C-A

129892832-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116169673-T-G

129893197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116170000-C-T

129893224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116170027-G-A

129893224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116170027-G-T

http://identifiers.org/hco/3/GRCh38#129893322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116170100-C-A

129893322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116170100-C-T

http://identifiers.org/hco/3/GRCh38#129893381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116170150-C-A

129893381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116170150-C-T

129893439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116170204-G-A

129893439-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116170204-G-T

http://identifiers.org/hco/3/GRCh38#129893592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116170319-C-A

129893592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5 prime UTR variant
orthologous variants: 116170319-C-T

http://identifiers.org/hco/3/GRCh38#129893601-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116170328-A-C

129893601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5 prime UTR variant
orthologous variants: 116170328-A-G

129893610-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5 prime UTR variant
orthologous variants: 116170337-T-A

129893610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5 prime UTR variant
orthologous variants: 116170337-T-C

129893610-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5 prime UTR variant
orthologous variants: 116170337-T-G

129893614-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5 prime UTR variant
orthologous variants: 116170341-G-C

129893631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5 prime UTR variant
orthologous variants: 116170358-G-A

129893631-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5 prime UTR variant
orthologous variants: 116170358-G-C

129893631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29116
most severe consequence: 5 prime UTR variant
orthologous variants: 116170358-G-T