72288586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101440693-T-C

72288711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101440610-C-T

72288792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101440525-G-T

http://identifiers.org/hco/11/GRCh38#72288795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#101440522-C-A

72288799-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101440518-T-G

72289313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101440322-T-C

72289313-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101440322-T-G

72289315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101440320-G-A

72289315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101440320-G-T

72289383-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101439661-A-T

72289384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101439659-T-C

http://identifiers.org/hco/11/GRCh38#72289408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#101439636-C-A

72289408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101439636-C-T

72289493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101439575-A-G

72292398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 3 prime UTR variant
orthologous variants: 101437660-T-C

72292544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 3 prime UTR variant
orthologous variants: 101437558-A-G

72292566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 3 prime UTR variant
orthologous variants: 101437537-C-T

http://identifiers.org/hco/11/GRCh38#72292855-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#101437351-A-C

http://identifiers.org/hco/11/GRCh38#72292900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#101437307-C-A

72292900-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 3 prime UTR variant
orthologous variants: 101437307-C-G

72292900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 3 prime UTR variant
orthologous variants: 101437307-C-T

72292923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 3 prime UTR variant
orthologous variants: 101437285-T-C

72292925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 3 prime UTR variant
orthologous variants: 101437283-G-A

72292925-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 3 prime UTR variant
orthologous variants: 101437283-G-C

72292925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 3 prime UTR variant
orthologous variants: 101437283-G-T

72292956-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 3 prime UTR variant
orthologous variants: 101437253-T-G

72292962-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 3 prime UTR variant
orthologous variants: 101437246-T-A

72292962-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 3 prime UTR variant
orthologous variants: 101437246-T-G

72292990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 3 prime UTR variant
orthologous variants: 101437219-C-T

http://identifiers.org/hco/11/GRCh38#72293040-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#101437171-A-C

72293045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 3 prime UTR variant
orthologous variants: 101437165-G-A

72293045-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 3 prime UTR variant
orthologous variants: 101437165-G-C

72293045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 3 prime UTR variant
orthologous variants: 101437165-G-T

72293057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 3 prime UTR variant
orthologous variants: 101437153-G-A

72293080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 3 prime UTR variant
orthologous variants: 101437130-A-G

http://identifiers.org/hco/11/GRCh38#72293096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#101437116-C-A

72293109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 3 prime UTR variant
orthologous variants: 101437103-A-G

http://identifiers.org/hco/11/GRCh38#72293542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#101436783-C-A

72293542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 101436783-C-T

72293584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 101436741-G-A

72293584-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 101436741-G-C

72293584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 101436741-G-T

72293653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101436668-T-C

http://identifiers.org/hco/11/GRCh38#72293711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#101436599-C-A

72293749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101436569-G-T

72294204-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101435754-G-C

72294205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101435753-G-A

72294206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101435752-C-T

72294621-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 101435377-T-G

http://identifiers.org/hco/11/GRCh38#72294748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#101435252-C-A

72294748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101435252-C-T

http://identifiers.org/hco/11/GRCh38#72294807-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#101435207-C-A

72294824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101435192-G-T

72294832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101435185-G-A

72295414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101434767-G-A

72295414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101434767-G-T

72295471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101434710-T-C

72295808-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101434417-T-A

72295808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101434417-T-C

72296389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101433324-G-T

72296406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101433305-T-C

72296631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101433111-C-T

72296928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101432911-C-T

72296997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101432850-T-C

72297111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101432760-A-G

72297719-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101432283-T-A

72297719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101432283-T-C

http://identifiers.org/hco/11/GRCh38#72297724-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#101432278-A-C

72297724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101432278-A-G

72297737-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101432265-T-A

72297776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101432227-G-A

72297866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101432139-G-A

72298041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101432003-C-T

72298121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101431909-G-A

72298201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101431824-C-T

72298407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101431651-C-T

72298775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101431527-G-A

72299696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101430490-G-A

72299709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101430477-A-G

72299710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101430476-T-C

72299710-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101430476-T-G

72299914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101430276-T-C

72300049-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101430157-T-G

72300279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101430041-A-G

72300399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101429932-G-A

72300604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101429760-G-A

72300625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101429738-G-A

72300888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101429489-A-G

72300926-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101429457-C-G

72301062-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101429290-C-G

72301948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 101428423-C-T

72302044-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101428091-C-G

72302102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101428036-G-T

72302109-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101428029-A-T

http://identifiers.org/hco/11/GRCh38#72302157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#101427994-C-A

http://identifiers.org/hco/11/GRCh38#72302203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#101427937-C-A

72302206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101427934-G-T

http://identifiers.org/hco/11/GRCh38#72302244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#101427875-C-A

72302244-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101427875-C-G

72302244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101427875-C-T

72302272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101427847-C-T

72302361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 101427764-A-G

72302451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101427683-C-T

72302496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101427659-G-T

72302509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101427646-C-T

http://identifiers.org/hco/11/GRCh38#72302539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#101427619-C-A

http://identifiers.org/hco/11/GRCh38#72302541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#101427617-C-A

72302541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101427617-C-T

72302590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101427563-G-T

http://identifiers.org/hco/11/GRCh38#72302713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#101427465-C-A

http://identifiers.org/hco/11/GRCh38#72303000-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#101427217-A-C

72303000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101427217-A-G

http://identifiers.org/hco/11/GRCh38#72303049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#101427171-C-A

72303119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101427112-C-T

72303553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101426784-C-T

72304153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101426188-T-C

72304395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101425943-A-G

72304503-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101425861-T-G

72304529-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101425839-G-T

http://identifiers.org/hco/11/GRCh38#72304697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#101425681-C-A

72304758-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101425628-T-A

72305047-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101425336-T-A

72305047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101425336-T-C

72305123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101425272-T-C

72305357-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101425051-T-G

72305484-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101424976-C-G

72306180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101424306-G-A

72306330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101424150-G-A

72306556-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101423956-G-C

http://identifiers.org/hco/11/GRCh38#72306570-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#101423944-A-C

72306761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101423808-A-G

72307087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101423537-G-T

72307096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101423528-T-C

72307096-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101423528-T-G

72307147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101423491-G-A

72307187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101423465-C-T

http://identifiers.org/hco/11/GRCh38#72307317-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#101423340-A-C

72307364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101423160-G-A

72307447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101423111-C-T

72307613-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101422953-C-G

72307715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101422874-T-C

72308206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101422536-G-A

72308231-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101422512-T-A

72308616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101422273-C-T

72309041-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101421881-G-C

72309208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101421749-G-A

72309587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101421473-G-A

72310824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101420340-G-A

72310824-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101420340-G-C

72310824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101420340-G-T

72310854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101420310-C-T

72311053-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101420111-T-A

72311053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101420111-T-C

72311201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101419963-G-T

72311241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101419924-C-T

72311248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101419917-G-A

72311331-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101419832-C-G

72312092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101419217-C-T

72312094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101419215-G-A

72312118-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101419197-T-G

72312188-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101419129-A-T

72312922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101418046-G-A

72313004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101417983-G-A

72314218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101416796-A-G

72314439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101416622-T-C

72314904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101416312-G-A

72315282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101415482-G-A

72315351-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101415427-G-C

72315481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101415300-C-T

72316990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101413023-G-T

http://identifiers.org/hco/11/GRCh38#72317072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#101412942-C-A

72317072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101412942-C-T

72317074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101412940-A-G

http://identifiers.org/hco/11/GRCh38#72317077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#101412936-C-A

72317108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 101412898-G-A

72317108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 101412898-G-T

72317111-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 101412895-C-G

72317111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 101412895-C-T

72317313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101412696-G-A

72317313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101412696-G-T

72317369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101412642-G-A

72318249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101412355-A-G

72319327-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101411257-A-T

72319393-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101411204-T-A

72319889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101410860-T-C

72320028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101410716-C-T

72320356-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101410401-G-C

72320723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101409841-A-G

72320853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101409723-T-C

72320877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101409692-T-C

72320944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101409544-C-T

72320995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101409489-G-A

72321008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101409476-C-T

72321298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101409173-G-A

72321703-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101408759-G-C

72321723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101408739-A-G

72322239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101408030-A-G

72322591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101407711-T-C

72323068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101407366-T-C

72324662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101406293-T-C

72324756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101406217-G-A

72324756-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101406217-G-C

72324886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101406092-C-T

72325360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101405621-C-T

72325476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101405487-G-A

72325787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101405191-A-G

72325867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101405083-A-G

http://identifiers.org/hco/11/GRCh38#72326039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#101404964-C-A

72326040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101404963-A-G

72326085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101404925-G-A

72326461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101404596-T-C

72326723-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101403794-T-G

http://identifiers.org/hco/11/GRCh38#72326766-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#101403750-A-C

72326766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101403750-A-G

72326991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101403602-G-T

72327025-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101403573-A-T

72327253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101403412-C-T

http://identifiers.org/hco/11/GRCh38#72327379-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#101403277-A-C

72327612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101403054-A-G

72327647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101403019-G-A

72327730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101402963-C-T

72328156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101402524-C-T

72328670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101402015-G-A

72328944-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101401762-G-C

72328947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101401759-A-G

72328947-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101401759-A-T

72329068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101401639-C-T

72329650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101400584-G-T

72329653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101400581-G-A

72329768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 101400475-G-A

72329768-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 101400475-G-C

72329768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 101400475-G-T

72329913-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101400328-G-C

http://identifiers.org/hco/11/GRCh38#72329952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#101400223-C-A

72329961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101400188-C-T

72330028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101400136-T-C

72330113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101400050-T-C

72330473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101399609-T-C

72330518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101399570-C-T

72331206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101399027-A-G

http://identifiers.org/hco/11/GRCh38#72332705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#101398450-C-A

72332705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101398450-C-T

72332714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101398441-G-A

72332939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101398050-T-C

72332944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101398045-T-C

72332957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101398032-G-A

72332957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101398032-G-T

72332966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101398023-T-C

72332993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101397994-C-T

72333009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101397980-A-G

72333009-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101397980-A-T

72333080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101397894-T-C

72333206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101397772-C-T

72333242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101397675-C-T

72333489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101397129-A-G

72333517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101397101-C-T

72333666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101396977-T-C

72333672-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101396971-T-G

http://identifiers.org/hco/11/GRCh38#72333849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#101396823-C-A

72333849-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101396823-C-G

72334479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101396204-C-T

72334932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101395760-G-A

72334932-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101395760-G-C

72335350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101395346-C-T

72337186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101394246-A-G

http://identifiers.org/hco/11/GRCh38#72337249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#101394173-C-A

72337249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101394173-C-T

72337262-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101394090-T-A

72337262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101394090-T-C

72337262-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101394090-T-G

http://identifiers.org/hco/11/GRCh38#72337274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#101394078-C-A

72337274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101394078-C-T

72337286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101394066-T-C

72337474-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101393887-T-A

72337496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101393865-C-T

72337811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101393625-G-A

72338778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101392856-T-C

72338841-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101392827-A-T

http://identifiers.org/hco/11/GRCh38#72339311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#101392383-C-A

72339334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101392360-T-C

72340174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101391302-C-T

72340270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101391206-G-A

72340599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101390880-T-C

72340716-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101390790-A-T

72341329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101390434-C-T

72341367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101390396-G-A

72341468-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101390114-T-A

72341512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101390075-C-T

72342269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101389368-G-A

72342272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101389365-G-A

72342320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101389310-C-T

72343278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101388328-A-G

72343348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101388267-G-T

72346577-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101384046-T-A

72346742-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101383990-T-A

72346742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101383990-T-C

72346752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101383980-T-C

72347550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101383364-G-A

72347567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101383347-A-G

http://identifiers.org/hco/11/GRCh38#72347784-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#101383146-A-C

http://identifiers.org/hco/11/GRCh38#72348090-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#101382858-A-C

72348137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101382808-T-C

72348238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101382710-G-A

http://identifiers.org/hco/11/GRCh38#72348247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#101382700-C-A

72348258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101382669-T-C

72348333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101382610-G-A

72348333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101382610-G-T

72348394-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101382553-C-G

72348571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101382401-G-A

72348571-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101382401-G-C

72348921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101382165-T-C

72349205-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101381924-G-C

http://identifiers.org/hco/11/GRCh38#72349781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#101381546-C-A

72349937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101381403-A-G

72349944-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101381396-A-T

72350173-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101381188-G-C

72350173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101381188-G-T

72350336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101380822-T-C

72350538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101380653-T-C

72350555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101380636-A-G

72351119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101379741-G-T

72351205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101379703-A-G

72351211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101379697-G-T

72351417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101379527-G-A

72351417-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101379527-G-C

http://identifiers.org/hco/11/GRCh38#72351441-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#101379503-C-A

72352840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101376914-G-T

72353302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101376491-G-T

http://identifiers.org/hco/11/GRCh38#72353332-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#101376461-A-C

72353332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101376461-A-G

72353337-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101376456-A-T

http://identifiers.org/hco/11/GRCh38#72353375-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#101376417-A-C

72354369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101375923-G-T

72354442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101375852-T-C

http://identifiers.org/hco/11/GRCh38#72354452-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#101375842-A-C

http://identifiers.org/hco/11/GRCh38#72354557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#101375763-C-A

72354559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101375761-T-C

72354738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101375610-A-G

72354738-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101375610-A-T

http://identifiers.org/hco/11/GRCh38#72354767-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#101375581-A-C

http://identifiers.org/hco/11/GRCh38#72354798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#101375556-C-A

72354819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101375538-A-G

72354933-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101375422-G-C

72355030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101375341-A-G

72355286-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101375100-T-G

72355288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101375098-A-G

72355312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101375080-A-G

72356734-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101373945-G-C

72356734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101373945-G-T

72356870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101373810-G-A

72356870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101373810-G-T

72356911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101373773-G-T

72357263-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101373532-G-T

72357439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101373368-A-G

72357962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101373138-G-A

72358256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101372857-T-C

http://identifiers.org/hco/11/GRCh38#72358556-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#101372452-A-C

http://identifiers.org/hco/11/GRCh38#72358798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#101372208-C-A

72358798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101372208-C-T

http://identifiers.org/hco/11/GRCh38#72358808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#101372198-C-A

72358808-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101372198-C-G

72358808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101372198-C-T

72358966-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101371952-T-A

72359161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101371252-G-A

http://identifiers.org/hco/11/GRCh38#72359199-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#101371215-A-C

72359199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101371215-A-G

72359199-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101371215-A-T

72359549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101370901-C-T

72359870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101370408-T-C

72359980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101370285-T-C

72360112-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101370165-T-G

72361159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101369497-T-C

72361434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101369078-C-T

72362004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101368510-G-A

72368318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101364782-C-T

72368477-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101364648-T-G

72368846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101364296-A-G

72368869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101364273-T-C

72369145-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101364029-C-G

72369145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101364029-C-T

72369157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101364017-T-C

72369559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101363682-G-T

72370174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101363067-T-C

72370381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101362816-T-C

72371724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101361784-A-G

72371754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101361754-C-T

72372108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101361299-C-T

72372196-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101361212-G-C

72372838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101360789-A-G

72372867-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101360768-A-T

72372925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 101360705-C-T

72373232-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101360391-T-A

72374075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101359903-C-T

72374127-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101359851-G-C

72374425-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101359567-G-C

72375561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101359152-C-T

72375800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101358943-C-T

72376549-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101358138-T-A

72376549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101358138-T-C

72377227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101357741-G-A

72377532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101357497-A-G

http://identifiers.org/hco/11/GRCh38#72377556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#101357473-C-A

72378065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101357223-A-G

72378241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101357124-A-G

72378780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101356935-C-T

http://identifiers.org/hco/11/GRCh38#72379404-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#101356459-A-C

72379494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101356376-T-C

72379954-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101356030-T-G

http://identifiers.org/hco/11/GRCh38#72380225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#101355844-C-A

72380225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101355844-C-T

72385434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101354762-T-C

72386094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101354221-T-C

72386099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101354216-T-C

72386226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101354116-C-T

72387443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101352860-T-C

72387489-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101352815-A-T

72387509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101352797-G-A

http://identifiers.org/hco/11/GRCh38#72387656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#101352650-C-A

72387656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101352650-C-T

72387784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101352560-T-C

72387831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101352513-G-A

72387909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101352424-A-G

72388666-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101351986-T-A

72388666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101351986-T-C

72388738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101351912-A-G

72389399-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101351522-T-A

http://identifiers.org/hco/11/GRCh38#72389588-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#101351348-A-C

72389603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101351342-G-A

72390040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101351181-G-A

72390059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101351163-A-G

72392156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101349752-T-C

72392162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101349746-G-A

72392174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101349734-G-A

72392182-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101349729-A-T

72392659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101349296-G-A

72392718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101349241-A-G

72393322-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101348637-T-A

72393322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101348637-T-C

72394047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101347002-A-G

72394830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101346314-C-T

72395847-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101345212-G-C

72395872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101345189-C-T

72397429-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101342548-T-G

72397497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101342480-T-C

72397500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101342477-A-G

72397637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101342371-C-T

http://identifiers.org/hco/11/GRCh38#72398913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#101340974-C-A

72399148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101340576-A-G

http://identifiers.org/hco/11/GRCh38#72399382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#101340123-C-A

72400822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101338500-C-T

72400868-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101338474-T-A

72400940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101338337-T-C

72401619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101337925-T-C

72401636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101337913-G-A

72401702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101337835-G-T

72402804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101336628-T-C

72403017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 101336528-T-C

72403017-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 101336528-T-G

72403054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101336491-T-C

72403081-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101336528-T-A

72403081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101336528-T-C

72403081-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101336528-T-G

72403277-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101336269-T-G

72404016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101335602-G-A

72404142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101335494-A-G

http://identifiers.org/hco/11/GRCh38#72407955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#101334188-C-A

72407955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101334188-C-T

http://identifiers.org/hco/11/GRCh38#72407984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#101334161-C-A

72407984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101334161-C-T

72408022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101334131-G-A

72408022-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101334131-G-T

http://identifiers.org/hco/11/GRCh38#72408066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#101334101-C-A

72408091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 101334077-T-C

72408104-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 101334067-G-C

72408104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 101334067-G-T

72408187-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 101334013-C-G

72408187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 101334013-C-T

http://identifiers.org/hco/11/GRCh38#72408267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#101333962-C-A

72408267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101333962-C-T

72408291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101333939-T-C

72408873-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101333639-G-C

72408918-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101333583-T-A

http://identifiers.org/hco/11/GRCh38#72410758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#101332385-C-A

72411365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101331842-G-A

72411707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101331307-G-T

72411826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101331184-G-T

72412092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101330920-G-A

72412092-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101330920-G-C

72412092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101330920-G-T

72412259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101330745-G-A

72412586-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101330467-C-G

72412586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101330467-C-T

72412856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101330211-A-G

72412960-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101330126-T-G

72414238-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101329055-C-G

72415643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101327661-T-C

72415836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101327495-T-C

72415889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101327446-C-T

72416066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101327243-G-A

72417494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101326769-G-T

72417587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101326678-G-T

72417679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101326574-C-T

72417942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101326387-T-C

72417977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101326352-G-A

72422852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101324878-T-C

http://identifiers.org/hco/11/GRCh38#72426278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#101323003-C-A

72426278-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101323003-C-G

72426490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101322791-T-C

72427350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101321537-G-A

72428461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101320595-C-T

72428520-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101320565-C-G

72428684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101320108-G-T

72428737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101320059-A-G

72428737-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101320059-A-T

72428740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101320056-C-T

72428748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101320048-G-T

72428773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101320025-T-C

http://identifiers.org/hco/11/GRCh38#72428888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#101319907-C-A

72428997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101318398-A-G

72428997-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101318398-A-T

72429002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101318393-G-A

http://identifiers.org/hco/11/GRCh38#72429050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, stop_lost
orthologous variants: http://identifiers.org/mco/7/GRCm39#101318345-C-A

72429320-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101318082-C-G

72429400-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101318000-A-T

72429446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101317954-A-G

72429545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101317082-C-T

72429651-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101317000-T-G

72430238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101316555-G-T

http://identifiers.org/hco/11/GRCh38#72430462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#101316358-C-A

72430462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101316358-C-T

72430463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101316357-G-A

72430463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101316357-G-T

http://identifiers.org/hco/11/GRCh38#72430523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#101316322-C-A

72430523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101316322-C-T

72430832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101316239-G-A

72430960-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101316127-T-G

72431410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101315807-A-G

72431607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101315482-G-A

72431611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101315478-G-A

72431707-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101315317-T-A

72432015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101314988-T-C

72432021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101314982-T-C

72432285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101314764-G-A

72432433-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101314636-C-G

72433137-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101313982-G-C

72433700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101313758-G-A

72433833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101313639-A-G

http://identifiers.org/hco/11/GRCh38#72433852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#101313621-C-A

72433852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101313621-C-T

http://identifiers.org/hco/11/GRCh38#72434000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#101313486-C-A

72434000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101313486-C-T

72434036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101313458-G-A

72434036-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101313458-G-C

72434036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101313458-G-T

72434167-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101313323-C-G

72434167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 101313323-C-T

72434213-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained, undefined
orthologous variants: 101313277-A-T

http://identifiers.org/hco/11/GRCh38#72434242-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#101313248-A-C

72434364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 101313126-C-T

http://identifiers.org/hco/11/GRCh38#72434512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#101312981-C-A

72434512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 101312981-C-T

http://identifiers.org/hco/11/GRCh38#72434566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#101312927-C-A

72434566-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 101312927-C-G

72434566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 101312927-C-T

72434671-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 101312822-G-C

72434671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30664
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 101312822-G-T