19882421-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 138641245-T-A

19882421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 138641245-T-C

19882433-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 138641232-T-A

19882433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 138641232-T-C

http://identifiers.org/hco/1/GRCh38#19882477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#138641177-C-A

19882477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 138641177-C-T

http://identifiers.org/hco/1/GRCh38#19882577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#138641073-C-A

19882577-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 138641073-C-G

19882577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 138641073-C-T

19882586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 138641064-G-A

19882586-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 138641064-G-C

19882586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 138641064-G-T

19882637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 138641013-G-A

19882637-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 138641013-G-C

19882637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, stop_gained, undefined
orthologous variants: 138641013-G-T

http://identifiers.org/hco/1/GRCh38#19882688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#138640965-C-A

19882688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, stop_gained, undefined
orthologous variants: 138640965-C-T

19882759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138640894-G-A

19882759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138640894-G-T

http://identifiers.org/hco/1/GRCh38#19882779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138640875-C-A

19882779-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138640875-C-G

19882779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138640875-C-T

19882784-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 138640871-T-A

19882784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 138640871-T-C

19882885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138640865-G-A

19882895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138640855-A-G

19883072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138640762-A-G

19883220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 138640676-G-A

http://identifiers.org/hco/1/GRCh38#19883250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138640654-C-A

http://identifiers.org/hco/1/GRCh38#19883254-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138640650-A-C

19883302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 138640600-C-T

19883350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 138640557-G-A

19883405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 138640510-G-A

19883448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 138640466-G-A

19883463-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 138640451-G-C

19883774-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 138640113-C-G

19883814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 138640101-G-T

19883836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 138640078-A-G

19884013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 138639958-C-T

19884015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 138639956-C-T

19884652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 138639292-A-G

19884940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 138638976-A-G

19885377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 138638633-C-T

19885416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 138638589-G-A

19885569-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 138638453-T-A

19888002-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 138638196-T-G

19888040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 138638154-A-G

19888105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 138638090-A-G

19888243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 138637964-T-C

19888445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 138637744-A-G

19888515-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 138637659-A-T

19889701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 138637485-T-C

19890161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, start_lost
orthologous variants: 138637122-T-C

http://identifiers.org/hco/1/GRCh38#19890567-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138636757-A-C

19890640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138636688-G-A

19890640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138636688-G-T

19890679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138636652-G-A

19890679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138636652-G-T

19890938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138636362-T-C

19891352-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138635866-A-T

19891432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138635690-C-T

19892167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138634834-A-G

19892330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138634717-A-G

19892414-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138634650-G-C

19892569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138634484-T-C

19892583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138634471-A-G

19892630-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138634420-C-G

19892643-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138634407-C-G

19892643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138634407-C-T

19892952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138633782-C-T

19893091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138633650-G-A

http://identifiers.org/hco/1/GRCh38#19893161-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138633594-A-C

19893172-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138633582-C-G

19893215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138633507-A-G

19893215-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138633507-A-T

19893317-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138633451-C-G

19893442-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138633362-C-G

19893518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138633274-G-A

19893628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138633220-C-T

19894208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138632732-T-C

19894243-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138632701-T-G

19894377-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 138632569-T-G

19894597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138632362-A-G

http://identifiers.org/hco/1/GRCh38#19894668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138632298-C-A

19894668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138632298-C-T

http://identifiers.org/hco/1/GRCh38#19895059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138631577-C-A

19895449-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138631261-C-G

19895449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138631261-C-T

19895585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138631126-G-A

19896280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138630362-A-G

19896345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138630295-T-C

19896467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138630185-G-T

19896476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138630177-G-T

19896530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138630125-G-A

19896573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138630098-G-A

19896573-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138630098-G-C

http://identifiers.org/hco/1/GRCh38#19896764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138629963-C-A

19896764-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138629963-C-G

19896764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138629963-C-T

19896978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138629756-C-T

19897370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138629415-A-G

http://identifiers.org/hco/1/GRCh38#19897408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138629384-C-A

19897408-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138629384-C-G

19897454-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138629358-T-A

19897454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138629358-T-C

19897562-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 138629261-G-C

19897660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 138629163-G-A

19903141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron variant
orthologous variants: 138626459-G-A

19903146-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron variant
orthologous variants: 138626455-C-G

19903310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron variant
orthologous variants: 138626286-C-T

19903322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron variant
orthologous variants: 138626281-G-A

19903391-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron variant
orthologous variants: 138626174-A-T

19903908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, undefined
orthologous variants: 138625755-G-A

19903917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron variant
orthologous variants: 138625747-G-A

19903952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, undefined
orthologous variants: 138625726-C-T

19904132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron variant
orthologous variants: 138625568-G-A

19904132-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron variant
orthologous variants: 138625568-G-C

19904132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron variant
orthologous variants: 138625568-G-T

http://identifiers.org/hco/1/GRCh38#19904480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138625281-C-A

19904480-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron variant
orthologous variants: 138625281-C-G

19904480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron variant
orthologous variants: 138625281-C-T

19904511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron variant
orthologous variants: 138625269-G-A

19904511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron variant
orthologous variants: 138625269-G-T

19904774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron variant
orthologous variants: 138625057-C-T

19904810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron variant
orthologous variants: 138625041-A-G

19904827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron variant
orthologous variants: 138625017-G-A

19904999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron variant
orthologous variants: 138624854-A-G

19906249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron variant
orthologous variants: 138624370-C-T

19906335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron variant
orthologous variants: 138624303-G-T

19906342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron variant
orthologous variants: 138624295-G-T

19906396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron variant
orthologous variants: 138624242-G-A

19906396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron variant
orthologous variants: 138624242-G-T

19906407-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron variant
orthologous variants: 138624231-T-G

19906445-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, missense_variant
orthologous variants: 138624193-T-A

19906445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 138624193-T-C

19906501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, missense_variant
orthologous variants: 138624140-G-A

19906507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, missense_variant
orthologous variants: 138624134-G-A

19906630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138624010-G-A

19906630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138624010-G-T

19906640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138624000-G-A

19906650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138623990-G-A

19906650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138623990-G-T

19906651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138623989-G-A

19906654-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138623986-G-C

19906665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138623956-G-T

19906704-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138623917-T-A

19906715-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138623908-T-G

19906716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138623907-T-C

http://identifiers.org/hco/1/GRCh38#19906838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138623810-C-A

19906838-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 138623810-C-G

19906838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 138623810-C-T

19906915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 138623739-T-C

19906915-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 138623739-T-G

http://identifiers.org/hco/1/GRCh38#19906948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138623724-C-A

19906948-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron variant
orthologous variants: 138623724-C-G

http://identifiers.org/hco/1/GRCh38#19906975-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138623696-A-C

19907173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron variant
orthologous variants: 138623543-A-G

http://identifiers.org/hco/1/GRCh38#19907301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138623420-C-A

19907301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron variant
orthologous variants: 138623420-C-T

19907561-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: intron variant
orthologous variants: 138623232-C-G

http://identifiers.org/hco/1/GRCh38#19907573-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138623220-A-C

19907573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: missense variant
orthologous variants: 138623220-A-G

19907618-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: missense variant
orthologous variants: 138623175-C-G

19907618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: missense variant
orthologous variants: 138623175-C-T

19907684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 138623109-A-G

http://identifiers.org/hco/1/GRCh38#19907773-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138623022-A-C

http://identifiers.org/hco/1/GRCh38#19907800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138623004-C-A

19907800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 3 prime UTR variant
orthologous variants: 138623004-C-T

19908020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 3 prime UTR variant
orthologous variants: 138622831-G-A

19908028-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 3 prime UTR variant
orthologous variants: 138622823-T-A

19908028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 3 prime UTR variant
orthologous variants: 138622823-T-C

19908053-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 3 prime UTR variant
orthologous variants: 138622798-T-A

19908053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 3 prime UTR variant
orthologous variants: 138622798-T-C

19908263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 3 prime UTR variant
orthologous variants: 138622595-A-G

19908448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 3 prime UTR variant
orthologous variants: 138622440-T-C

19908515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 3 prime UTR variant
orthologous variants: 138622387-G-A

19908585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 3 prime UTR variant
orthologous variants: 138622325-G-A

19908585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 3 prime UTR variant
orthologous variants: 138622325-G-T

19908744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 3 prime UTR variant
orthologous variants: 138622177-T-C

19909011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 3 prime UTR variant
orthologous variants: 138621823-A-G

19909013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 3 prime UTR variant
orthologous variants: 138621821-G-T

19909169-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 3 prime UTR variant
orthologous variants: 138621673-T-A

19909181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 3 prime UTR variant
orthologous variants: 138621668-T-C

http://identifiers.org/hco/1/GRCh38#19909206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138621642-C-A

19909206-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 3 prime UTR variant
orthologous variants: 138621642-C-G

19909236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 3 prime UTR variant
orthologous variants: 138621614-G-T

19909339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 3 prime UTR variant
orthologous variants: 138621514-G-T

http://identifiers.org/hco/1/GRCh38#19909481-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138621428-A-C

19909616-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 3 prime UTR variant
orthologous variants: 138621332-T-A

19909616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 3 prime UTR variant
orthologous variants: 138621332-T-C

http://identifiers.org/hco/1/GRCh38#19909808-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138621057-A-C

19909808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 3 prime UTR variant
orthologous variants: 138621057-A-G

http://identifiers.org/hco/1/GRCh38#19910344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138620589-C-A

19910516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 3 prime UTR variant
orthologous variants: 138620434-T-C

19910552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 3 prime UTR variant
orthologous variants: 138620403-C-T

19910582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 3 prime UTR variant
orthologous variants: 138620379-A-G

http://identifiers.org/hco/1/GRCh38#19910605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138620357-C-A

19910721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 3 prime UTR variant
orthologous variants: 138620243-G-A

19910721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 3 prime UTR variant
orthologous variants: 138620243-G-T

19910760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 3 prime UTR variant
orthologous variants: 138620202-A-G

19910811-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 3 prime UTR variant
orthologous variants: 138620168-A-T

19910819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 3 prime UTR variant
orthologous variants: 138620160-G-T

http://identifiers.org/hco/1/GRCh38#19910949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138620054-C-A

19910949-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 3 prime UTR variant
orthologous variants: 138620054-C-G

19911121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 3 prime UTR variant
orthologous variants: 138619896-G-A

19911121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 3 prime UTR variant
orthologous variants: 138619896-G-T

19911390-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 3 prime UTR variant
orthologous variants: 138619742-T-A

19911438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 3 prime UTR variant
orthologous variants: 138619704-G-A

19911438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 3 prime UTR variant
orthologous variants: 138619704-G-T

http://identifiers.org/hco/1/GRCh38#19911452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138619690-C-A

19911452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 3 prime UTR variant
orthologous variants: 138619690-C-T

19911454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 3 prime UTR variant
orthologous variants: 138619688-A-G

19911467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 3 prime UTR variant
orthologous variants: 138619672-G-A

19911496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 3 prime UTR variant
orthologous variants: 138619652-T-C

http://identifiers.org/hco/1/GRCh38#19912162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138619157-C-A

19912294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 3 prime UTR variant
orthologous variants: 138619051-A-G

19912396-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 3 prime UTR variant
orthologous variants: 138618961-T-A

19912396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 3 prime UTR variant
orthologous variants: 138618961-T-C

19912476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 3 prime UTR variant
orthologous variants: 138618885-T-C

19912479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 3 prime UTR variant
orthologous variants: 138618882-C-T

19912487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 3 prime UTR variant
orthologous variants: 138618877-G-T

http://identifiers.org/hco/1/GRCh38#19912499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#138618861-C-A

19912514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 3 prime UTR variant
orthologous variants: 138618846-G-T

19912518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29038
most severe consequence: 3 prime UTR variant
orthologous variants: 138618842-T-C