169066503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 5 prime UTR variant
orthologous variants: 69207728-T-C

169066508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 5 prime UTR variant
orthologous variants: 69207733-A-G

http://identifiers.org/hco/2/GRCh38#169066550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69207773-C-A

169066663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 5 prime UTR variant
orthologous variants: 69207884-C-T

169066733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69207947-G-T

169066888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69208107-C-T

169066915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69208134-G-A

169066915-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69208134-G-C

169066915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69208134-G-T

http://identifiers.org/hco/2/GRCh38#169066948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69208155-C-A

169066972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69208185-G-A

169066972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69208185-G-T

169066987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69208199-G-A

169066987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69208199-G-T

169066998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69208210-A-G

169067027-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69208239-A-T

169067045-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 69208253-T-A

169067045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 69208253-T-C

169067045-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 69208253-T-G

169067068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 69208277-G-T

169067121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 69208319-G-T

169067141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 69208339-A-G

169067155-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 69208353-A-T

http://identifiers.org/hco/2/GRCh38#169067184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69208367-C-A

169067184-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 69208367-C-G

http://identifiers.org/hco/2/GRCh38#169067292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69208472-C-A

169067318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69208497-G-A

169067318-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69208497-G-C

169067339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69208524-G-A

http://identifiers.org/hco/2/GRCh38#169067350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69208535-C-A

169067350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69208535-C-T

http://identifiers.org/hco/2/GRCh38#169067577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69208733-C-A

169068014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69209689-C-T

169068059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69209729-A-G

169068114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69209784-G-A

http://identifiers.org/hco/2/GRCh38#169068203-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69209865-A-C

169068827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69210207-G-A

169068867-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69210256-T-G

169068956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69210333-A-G

169069005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69210371-G-A

169069005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69210371-G-T

169069423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69210698-C-T

169069429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69210704-C-T

169069493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 69210766-T-C

169069609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 69210866-A-G

169069609-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 69210866-A-T

169069681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 69210939-A-G

169069723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69210981-T-C

169069739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69210997-A-G

http://identifiers.org/hco/2/GRCh38#169069790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69211032-C-A

169069790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69211032-C-T

169069880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69211109-G-A

169069892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69211120-C-T

169069983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69211212-T-C

169069983-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69211212-T-G

169069988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69211217-T-C

169070151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 69211399-G-A

169070151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 69211399-G-T

169070184-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 69211425-G-T

169070260-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 69211495-A-T

169070330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 69211550-A-G

http://identifiers.org/hco/2/GRCh38#169070395-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69211603-A-C

169070466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 69211630-C-T

169070497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 69211661-G-A

169070533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 69211691-T-C

169070640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 69211799-A-G

169070696-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 69211845-T-A

http://identifiers.org/hco/2/GRCh38#169071232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69212040-C-A

169071365-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69212160-G-C

169071713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69212379-T-C

http://identifiers.org/hco/2/GRCh38#169072002-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69212684-A-C

169072002-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69212684-A-T

http://identifiers.org/hco/2/GRCh38#169072028-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69212715-C-A

169072028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69212715-C-T

http://identifiers.org/hco/2/GRCh38#169072033-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69212720-C-A

http://identifiers.org/hco/2/GRCh38#169072394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69213096-C-A

http://identifiers.org/hco/2/GRCh38#169072499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69213178-C-A

169072587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 69213260-A-G

169072728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 69213377-T-C

http://identifiers.org/hco/2/GRCh38#169072776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69213425-C-A

169072776-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 69213425-C-G

169072788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 69213437-G-T

http://identifiers.org/hco/2/GRCh38#169072809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69213799-C-A

169072809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 69213799-C-T

169072810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 69213800-A-G

169072810-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 69213800-A-T

169072934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 69213929-A-G

169072937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 69213932-T-C

169072998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 69213999-G-A

169073162-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 69214123-G-C

169073163-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 69214124-T-A

169073501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 69215700-T-C

169073542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 69215746-C-T

169073727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 69215923-G-A

169074208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 69216351-C-T

169074341-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 69216439-T-G

169074389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 69216487-G-T

169074538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69216635-G-T

169074639-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69216720-T-A

169074795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69216874-G-A

http://identifiers.org/hco/2/GRCh38#169074873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69216957-C-A

http://identifiers.org/hco/2/GRCh38#169075096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69217226-C-A

169075116-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69217239-T-G

169075216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69217326-C-T

169077312-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69219353-T-A

169077458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69219626-A-G

http://identifiers.org/hco/2/GRCh38#169077512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69219673-C-A

169077624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69219777-G-A

169077656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69219806-G-A

http://identifiers.org/hco/2/GRCh38#169077804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69219934-C-A

169077910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69220122-T-C

169077951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69220162-C-T

169077994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69220204-G-A

169078092-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69220278-C-G

169078225-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69220412-G-C

169078302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69220487-G-T

169078308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69220493-A-G

http://identifiers.org/hco/2/GRCh38#169078326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69220511-C-A

169078457-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69220615-G-C

169078457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69220615-G-T

169078590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69220738-C-T

169078600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69220754-G-A

http://identifiers.org/hco/2/GRCh38#169079875-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69221231-A-C

169079875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69221231-A-G

169079894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69221250-A-G

http://identifiers.org/hco/2/GRCh38#169079904-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69221260-A-C

169079909-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69221265-G-C

169079914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69221270-G-A

169079914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69221270-G-T

169079924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69221280-A-G

169079929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69221285-G-A

169079929-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69221285-G-C

169079934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69221290-A-G

169079939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69221295-G-A

169079944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69221300-A-G

169079944-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69221300-A-T

169079949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69221305-G-A

169079975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69221331-G-A

169079980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69221336-A-G

169079985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69221341-G-A

http://identifiers.org/hco/2/GRCh38#169079995-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69221351-A-C

169079995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69221351-A-G

169080005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69221361-G-A

169080010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69221366-A-G

http://identifiers.org/hco/2/GRCh38#169080015-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69221371-A-C

169080015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69221371-A-G

169080243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69221806-T-C

169080293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69221861-G-T

169080400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69221961-T-C

169080446-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69222009-C-G

http://identifiers.org/hco/2/GRCh38#169080531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69222072-C-A

http://identifiers.org/hco/2/GRCh38#169080722-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69222266-A-C

http://identifiers.org/hco/2/GRCh38#169081041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69222527-C-A

http://identifiers.org/hco/2/GRCh38#169081143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69222724-C-A

169081153-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron_variant, splice_donor_variant
orthologous variants: 69222855-G-C

169081170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69222872-G-A

169081170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69222872-G-T

169081184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69222886-G-A

169081298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69222994-T-C

169081298-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69222994-T-G

169081299-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69222995-T-G

169081300-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69222996-T-A

169081300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69222996-T-C

169081301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69222997-A-G

169081301-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69222997-A-T

169081516-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 69223189-C-G

169081516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 69223189-C-T

http://identifiers.org/hco/2/GRCh38#169081528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69223201-C-A

169081528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 69223201-C-T

169081541-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 5_prime_UTR_variant, intron_variant, stop_gained
orthologous variants: 69223211-T-A

169081543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 69223213-T-C

169081546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 69223216-A-G

169081617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 69223289-T-C

169081677-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 69223349-T-A

169081677-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 69223349-T-G

169081698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 69223370-G-A

http://identifiers.org/hco/2/GRCh38#169081909-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69223583-A-C

169081909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69223583-A-G

169081931-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69223605-T-A

169081931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69223605-T-C

http://identifiers.org/hco/2/GRCh38#169081969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69223665-C-A

169082036-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69223731-G-C

169082036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69223731-G-T

169082298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69223952-A-G

169082631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69224158-C-T

169083314-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69224612-T-A

169083314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69224612-T-C

169083429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 69224727-G-A

169083447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 69224745-G-A

169083507-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: missense variant
orthologous variants: 69224805-T-G

169083608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69224906-T-C

http://identifiers.org/hco/2/GRCh38#169083615-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69224908-A-C

169083627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69224920-C-T

169088804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69225131-G-A

169088932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69225243-A-G

169088932-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69225243-A-T

169088963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69225274-G-T

169089234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69225529-G-T

169089278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69225573-T-C

169089763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69226010-T-C

169089854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69226103-G-A

169089885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69226138-C-T

169090061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69226323-A-G

169090115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69226379-T-C

169090271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69226539-T-C

169090352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69226614-G-T

169091366-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69227402-A-T

169091397-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69227429-G-C

169091397-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69227429-G-T

169091541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69227568-C-T

169091671-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69227700-T-G

169091835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: synonymous variant
orthologous variants: 69228005-A-G

http://identifiers.org/hco/2/GRCh38#169091986-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69228159-A-C

169092016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69228189-T-C

169092017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69228190-T-C

169092017-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69228190-T-G

169092076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69228220-G-A

169092193-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69228331-T-G

169092241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69228382-G-A

169092329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69228468-T-C

169092435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69228578-G-A

http://identifiers.org/hco/2/GRCh38#169092505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69228648-C-A

169092879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69229003-T-C

169092980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69229085-A-G

169093126-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69229232-C-G

169093178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69229284-C-T

169093343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69229446-C-T

169093351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69229454-C-T

169093354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69229457-A-G

169093359-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69229462-T-A

169093373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69229476-G-A

169093467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69229557-A-G

169093528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69229635-C-T

169093551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69229658-C-T

169093584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69229691-G-A

169093584-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69229691-G-C

169093634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69229741-C-T

169093936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69230177-C-T

169093964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69230204-T-C

169094083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69230317-T-C

169094414-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69230664-C-G

169094867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69230947-T-C

169095027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69231071-A-G

http://identifiers.org/hco/2/GRCh38#169095067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69231106-C-A

169095125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69231163-T-C

169095221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69231246-T-C

169095436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69231465-G-A

169095436-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69231465-G-C

169095436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69231465-G-T

http://identifiers.org/hco/2/GRCh38#169095473-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69231504-C-A

169095473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: intron variant
orthologous variants: 69231504-C-T

169095596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: synonymous variant
orthologous variants: 69231630-G-A

169095596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: synonymous variant
orthologous variants: 69231630-G-T

169095800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 3 prime UTR variant
orthologous variants: 69231834-T-C

169095813-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 3 prime UTR variant
orthologous variants: 69231847-T-A

169095842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 3 prime UTR variant
orthologous variants: 69231873-A-G

http://identifiers.org/hco/2/GRCh38#169095868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69231899-C-A

169095868-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 3 prime UTR variant
orthologous variants: 69231899-C-G

169095924-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 3 prime UTR variant
orthologous variants: 69231934-T-A

http://identifiers.org/hco/2/GRCh38#169096012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69232022-C-A

169096012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 3 prime UTR variant
orthologous variants: 69232022-C-T

169096019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 3 prime UTR variant
orthologous variants: 69232029-G-A

169096019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 3 prime UTR variant
orthologous variants: 69232029-G-T

169096134-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 3 prime UTR variant
orthologous variants: 69232128-T-A

169096134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 3 prime UTR variant
orthologous variants: 69232128-T-C

169096149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16888
most severe consequence: 3 prime UTR variant
orthologous variants: 69232143-A-G