69483542-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80738282-G-C

69483588-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80738329-T-G

http://identifiers.org/hco/14/GRCh38#69483692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#80738435-C-A

69483904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80738681-G-T

http://identifiers.org/hco/14/GRCh38#69484178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#80738915-C-A

69484422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, undefined
orthologous variants: 80739146-T-C

69484462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80739184-G-A

69484606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, undefined
orthologous variants: 80739324-G-T

http://identifiers.org/hco/14/GRCh38#69484611-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#80739329-A-C

69484611-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, undefined
orthologous variants: 80739329-A-T

69484635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80739353-G-A

69484635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80739353-G-T

69484708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80739414-G-T

http://identifiers.org/hco/14/GRCh38#69484710-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#80739416-C-A

69484741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80739447-G-A

69484741-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80739447-G-C

69484741-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80739447-G-T

http://identifiers.org/hco/14/GRCh38#69484755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#80739461-C-A

69484755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80739461-C-T

69484847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80739546-G-A

69484847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80739546-G-T

http://identifiers.org/hco/14/GRCh38#69485061-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/12/GRCm39#80739748-C-A

69485061-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 80739748-C-G

69485128-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80739817-C-G

69485128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80739817-C-T

http://identifiers.org/hco/14/GRCh38#69485346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#80740053-C-A

69485346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80740053-C-T

http://identifiers.org/hco/14/GRCh38#69485595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#80740278-C-A

69485595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80740278-C-T

69485959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80740529-A-G

http://identifiers.org/hco/14/GRCh38#69485993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#80740565-C-A

69486103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80740665-C-T

69486391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80740923-G-A

69486542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80741161-T-C

69486646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80741228-G-A

69486773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80741353-G-T

69486955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80741452-A-G

http://identifiers.org/hco/14/GRCh38#69487007-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#80741495-A-C

69487223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80741657-A-G

69487290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80741718-C-T

69487299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80741726-G-A

69487490-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80741914-A-T

69487588-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80742008-C-G

69487672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80742091-C-T

69487773-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80742169-A-T

http://identifiers.org/hco/14/GRCh38#69491000-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#80742330-A-C

69491067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80742397-G-T

69491136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80742460-G-A

http://identifiers.org/hco/14/GRCh38#69491481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#80745309-C-A

69491481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80745309-C-T

69491536-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80745357-G-C

69491536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80745357-G-T

69491650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80745679-C-T

69491657-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80745685-T-G

69491689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80745717-G-A

http://identifiers.org/hco/14/GRCh38#69491749-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#80745778-A-C

69491832-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80745817-C-G

69491832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80745817-C-T

69491870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80745856-T-C

69491877-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80745863-A-T

69492099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80746055-T-C

69492210-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80746169-C-G

69492256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80746213-C-T

69492395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80746539-C-T

69492406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80746550-C-T

69492413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80746557-T-C

69492458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80746600-C-T

69492604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80746768-C-T

69492806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80746972-G-T

http://identifiers.org/hco/14/GRCh38#69492858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#80746984-C-A

69492966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80746997-C-T

http://identifiers.org/hco/14/GRCh38#69493027-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#80747049-A-C

69493035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80747057-G-A

69493164-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80747170-C-G

69493231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80747226-T-C

69493303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80747286-G-A

http://identifiers.org/hco/14/GRCh38#69493342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#80747329-C-A

69493777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80748122-A-G

69493799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80748145-G-A

69493892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80748230-C-T

69493916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80748249-G-T

69493989-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80748283-G-C

69493990-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80748284-G-C

69493990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80748284-G-T

69494212-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80748479-T-G

http://identifiers.org/hco/14/GRCh38#69494257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#80748504-C-A

69494257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80748504-C-T

69494260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80748507-T-C

69494415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80748643-T-C

69494604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80748811-A-G

69494613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80748820-A-G

69494643-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80748844-T-G

69494679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80748867-G-A

http://identifiers.org/hco/14/GRCh38#69494829-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#80749019-A-C

69494914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80749075-G-A

69494914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80749075-G-T

http://identifiers.org/hco/14/GRCh38#69495092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#80749169-C-A

69495318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80749319-C-T

69495465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80749509-A-G

69495469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80749513-C-T

69495494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80749538-T-C

69495579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80749615-G-A

69495611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80749643-C-T

69495722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80749765-T-C

69496902-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80750492-T-G

http://identifiers.org/hco/14/GRCh38#69496908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#80750498-C-A

http://identifiers.org/hco/14/GRCh38#69497115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#80750636-C-A

69497115-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80750636-C-G

69497115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80750636-C-T

69497138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80750659-T-C

69497274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80750789-G-A

69497278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80750793-G-A

69497326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80750822-T-C

69497392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80750887-A-G

69498408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80751206-G-T

http://identifiers.org/hco/14/GRCh38#69498491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#80751310-C-A

69498491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80751310-C-T

69499077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80751446-G-A

69499223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80751589-G-A

69499223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80751589-G-T

69499231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80751597-A-G

69499393-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80751733-G-C

69499661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80751929-G-A

69500009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80752167-T-C

69500009-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80752167-T-G

http://identifiers.org/hco/14/GRCh38#69500038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#80752197-C-A

69500038-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80752197-C-G

69500038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80752197-C-T

69500211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80752414-G-A

69500280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80752467-G-A

69500280-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80752467-G-C

69500337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80752523-T-C

69500338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80752524-G-T

69500381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80752573-T-C

69500401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80752604-G-A

69500401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80752604-G-T

http://identifiers.org/hco/14/GRCh38#69500514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#80752714-C-A

69500514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80752714-C-T

69500532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80752732-C-T

69500548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80752749-G-A

http://identifiers.org/hco/14/GRCh38#69500585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#80752787-C-A

69500669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80752871-G-T

69500721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80752925-G-T

69500809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80753006-G-T

69500810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80753007-G-A

69500810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80753007-G-T

69500852-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80753109-T-G

69500891-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 80753147-T-G

69500897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 80753153-G-A

69500897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 80753153-G-T

http://identifiers.org/hco/14/GRCh38#69500998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#80753244-C-A

69500998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80753244-C-T

69501011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80753257-G-T

http://identifiers.org/hco/14/GRCh38#69501016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#80753261-C-A

69501042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80753283-G-T

http://identifiers.org/hco/14/GRCh38#69501058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#80753297-C-A

69501058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80753297-C-T

69501060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80753299-G-A

69501060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80753299-G-T

69501074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80753313-G-T

69501083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80753322-A-G

69501129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80753370-G-A

69501144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80753386-G-A

69501144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80753386-G-T

69501212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80753474-C-T

http://identifiers.org/hco/14/GRCh38#69501226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#80753488-C-A

69501226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80753488-C-T

69501268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80753529-T-C

http://identifiers.org/hco/14/GRCh38#69501456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#80753684-C-A

http://identifiers.org/hco/14/GRCh38#69501567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#80753784-C-A

69501567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80753784-C-T

69501649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80753861-T-C

69501649-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80753861-T-G

http://identifiers.org/hco/14/GRCh38#69501670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#80753886-C-A

http://identifiers.org/hco/14/GRCh38#69501730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#80753942-C-A

69501841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80754058-G-T

69501966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80754165-A-G

http://identifiers.org/hco/14/GRCh38#69502002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#80754200-C-A

69502002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80754200-C-T

69502004-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80754202-T-A

69502004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80754202-T-C

69502082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80754268-G-A

69502082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80754268-G-T

69502198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80754395-G-T

http://identifiers.org/hco/14/GRCh38#69502250-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#80754451-A-C

69502276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80754476-G-A

69502276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80754476-G-T

69502281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80754481-T-C

http://identifiers.org/hco/14/GRCh38#69502587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#80754739-C-A

69502587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80754739-C-T

69502651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80754790-A-G

69502706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80754849-A-G

69502706-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80754849-A-T

69502741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80754883-G-A

69502741-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80754883-G-T

69502744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80754886-C-T

69502803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80754932-G-T

69503034-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80755166-T-A

69503034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80755166-T-C

http://identifiers.org/hco/14/GRCh38#69503039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#80755167-C-A

http://identifiers.org/hco/14/GRCh38#69503043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#80755171-C-A

69503043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80755171-C-T

69503046-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80755174-T-A

69503046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80755174-T-C

69503076-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80755223-T-G

http://identifiers.org/hco/14/GRCh38#69503206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#80755300-C-A

69503213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80755308-T-C

69503219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80755314-T-C

69503257-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80755385-T-G

69503275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80755403-C-T

69503355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80755485-G-A

69503355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80755485-G-T

69503989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80755579-C-T

http://identifiers.org/hco/14/GRCh38#69504365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#80755978-C-A

69504365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80755978-C-T

http://identifiers.org/hco/14/GRCh38#69504418-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#80756033-A-C

69504481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80756095-C-T

69504588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80756198-A-G

69504829-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80756416-C-G

69505424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80756993-G-A

69505478-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80757042-T-G

69505635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80757188-A-G

69505758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, undefined
orthologous variants: 80757276-A-G

69505810-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, undefined
orthologous variants: 80757327-G-C

69505837-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, undefined
orthologous variants: 80757354-C-G

69518744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80761139-G-A

69519185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80761528-T-C

69519223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80761570-G-T

69519289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80761632-T-C

69519289-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80761632-T-G

69521455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80763200-G-A

69521503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80763240-G-A

69521632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80763362-C-T

69521665-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80763401-T-A

69521858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80763576-A-G

69521978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80763715-A-G

http://identifiers.org/hco/14/GRCh38#69522202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#80763924-C-A

69522202-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80763924-C-G

69522202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80763924-C-T

69522236-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80763951-G-C

69522236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80763951-G-T

http://identifiers.org/hco/14/GRCh38#69522265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#80763979-C-A

69522375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 80764087-G-A

69522375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 80764087-G-T

69522651-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80764920-G-C

69522693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80764964-G-A

69522850-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80765120-T-A

69524108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80765583-C-T

69524289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: synonymous variant
orthologous variants: 80765747-G-A

69524289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: missense variant
orthologous variants: 80765747-G-T

69524325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80765783-G-A

69524400-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80765827-G-C

69524400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80765827-G-T

69524461-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80765887-T-A

69524461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80765887-T-C

69524487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80765911-T-C

69524519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80765943-T-C

http://identifiers.org/hco/14/GRCh38#69524612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#80766038-C-A

69524612-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80766038-C-G

69524655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80766069-G-A

http://identifiers.org/hco/14/GRCh38#69524750-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#80766160-A-C

69524811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80766224-G-A

69525197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80766538-T-C

69525332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80766657-G-A

69525492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80766876-G-A

69525851-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80767267-T-A

69525851-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80767267-T-G

69525923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80767338-C-T

69526131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80767556-G-A

http://identifiers.org/hco/14/GRCh38#69526138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#80767563-C-A

69526138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80767563-C-T

69526164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80767579-G-A

69526164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80767579-G-T

http://identifiers.org/hco/14/GRCh38#69526178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#80767593-C-A

69526178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80767593-C-T

http://identifiers.org/hco/14/GRCh38#69526189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#80767604-C-A

69526211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80767624-T-C

69526211-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80767624-T-G

69526226-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80767639-T-A

69526226-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80767639-T-G

69526531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80767858-C-T

69526559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80767886-G-A

69526628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80767936-A-G

69526629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80767937-G-T

69526724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: synonymous variant
orthologous variants: 80768014-G-A

69526781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: synonymous variant
orthologous variants: 80768071-G-A

69526781-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: synonymous variant
orthologous variants: 80768071-G-C

69526781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: synonymous variant
orthologous variants: 80768071-G-T

69526814-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: synonymous variant
orthologous variants: 80768104-T-G

http://identifiers.org/hco/14/GRCh38#69527357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#80768392-C-A

69527357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80768392-C-T

69527440-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80768467-T-G

69527472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80768489-G-A

69527472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80768489-G-T

http://identifiers.org/hco/14/GRCh38#69527665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#80768635-C-A

69527665-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80768635-C-G

69527665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80768635-C-T

http://identifiers.org/hco/14/GRCh38#69527688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#80768657-C-A

69527688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80768657-C-T

69527895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: synonymous variant
orthologous variants: 80768832-C-T

69527928-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: missense variant
orthologous variants: 80768865-T-G

69527953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80768885-G-A

69527953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80768885-G-T

69528029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80768944-A-G

69528061-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80768976-T-A

69528061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80768976-T-C

http://identifiers.org/hco/14/GRCh38#69528134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#80768991-C-A

69528240-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron variant
orthologous variants: 80769083-G-C

69528245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 80769088-C-T

69528406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: missense variant
orthologous variants: 80769246-G-A

69528406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: missense variant
orthologous variants: 80769246-G-T

69528427-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: 3 prime UTR variant
orthologous variants: 80769267-T-G

69528450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: 3 prime UTR variant
orthologous variants: 80769290-C-T

http://identifiers.org/hco/14/GRCh38#69528613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#80769559-C-A

http://identifiers.org/hco/14/GRCh38#69528636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#80769581-C-A

69528636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: 3 prime UTR variant
orthologous variants: 80769581-C-T

69528644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: 3 prime UTR variant
orthologous variants: 80769589-A-G

69528740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: 3 prime UTR variant
orthologous variants: 80769667-G-A

69528740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: 3 prime UTR variant
orthologous variants: 80769667-G-T

http://identifiers.org/hco/14/GRCh38#69528744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#80769671-C-A

69528744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: 3 prime UTR variant
orthologous variants: 80769671-C-T

69528756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: 3 prime UTR variant
orthologous variants: 80769677-G-T

69528786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: 3 prime UTR variant
orthologous variants: 80769694-G-A

69528786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: 3 prime UTR variant
orthologous variants: 80769694-G-T

69528824-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: 3 prime UTR variant
orthologous variants: 80769723-T-A

69528824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: 3 prime UTR variant
orthologous variants: 80769723-T-C

69528841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: 3 prime UTR variant
orthologous variants: 80769740-G-A

69528841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: 3 prime UTR variant
orthologous variants: 80769740-G-T

69528931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: 3 prime UTR variant
orthologous variants: 80769786-C-T

69528994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: 3 prime UTR variant
orthologous variants: 80769842-A-G

69528999-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: 3 prime UTR variant
orthologous variants: 80769850-C-G

69528999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: 3 prime UTR variant
orthologous variants: 80769850-C-T

69529021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: 3 prime UTR variant
orthologous variants: 80769870-T-C

69529029-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: 3 prime UTR variant
orthologous variants: 80769878-T-G

69529113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: 3 prime UTR variant
orthologous variants: 80769951-G-A

69529140-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: 3 prime UTR variant
orthologous variants: 80769984-C-G

69529140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: 3 prime UTR variant
orthologous variants: 80769984-C-T

http://identifiers.org/hco/14/GRCh38#69529187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#80770029-C-A

http://identifiers.org/hco/14/GRCh38#69529239-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#80770070-A-C

69529239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: 3 prime UTR variant
orthologous variants: 80770070-A-G

69529304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: 3 prime UTR variant
orthologous variants: 80770091-G-A

69529304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: 3 prime UTR variant
orthologous variants: 80770091-G-T

69529309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: 3 prime UTR variant
orthologous variants: 80770096-G-A

69529309-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: 3 prime UTR variant
orthologous variants: 80770096-G-T

http://identifiers.org/hco/14/GRCh38#69529424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#80770115-C-A

69529534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: 3 prime UTR variant
orthologous variants: 80770142-A-G

69529535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: 3 prime UTR variant
orthologous variants: 80770143-G-T

http://identifiers.org/hco/14/GRCh38#69529536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#80770144-C-A

69529536-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: 3 prime UTR variant
orthologous variants: 80770144-C-G

69529536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: 3 prime UTR variant
orthologous variants: 80770144-C-T

69529721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: 3 prime UTR variant
orthologous variants: 80770199-G-T

69529735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: 3 prime UTR variant
orthologous variants: 80770213-A-G

69529750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: 3 prime UTR variant
orthologous variants: 80770228-G-A

69529750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: 3 prime UTR variant
orthologous variants: 80770228-G-T

http://identifiers.org/hco/14/GRCh38#69529899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#80770376-C-A

69530010-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: 3 prime UTR variant
orthologous variants: 80770458-T-A

69530010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: 3 prime UTR variant
orthologous variants: 80770458-T-C

69530281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: 3 prime UTR variant
orthologous variants: 80770769-G-A

69530281-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: 3 prime UTR variant
orthologous variants: 80770769-G-T

69530296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: 3 prime UTR variant
orthologous variants: 80770784-C-T

69530320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: 3 prime UTR variant
orthologous variants: 80770813-T-C

69530320-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: 3 prime UTR variant
orthologous variants: 80770813-T-G

http://identifiers.org/hco/14/GRCh38#69530353-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#80770878-C-A

http://identifiers.org/hco/14/GRCh38#69530365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#80770881-C-A

69530491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: 3 prime UTR variant
orthologous variants: 80771002-C-T

69531026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: 3 prime UTR variant
orthologous variants: 80771348-A-G

69531142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: 3 prime UTR variant
orthologous variants: 80771390-C-T

69531146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: 3 prime UTR variant
orthologous variants: 80771394-T-C

69531232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: 3 prime UTR variant
orthologous variants: 80771422-G-A

http://identifiers.org/hco/14/GRCh38#69531323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#80771516-C-A

69531504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20148
most severe consequence: 3 prime UTR variant
orthologous variants: 80771684-C-T